GENETICS INSTITUTE OF AMERICA LABORATORY FL1 CORP
NPI 1023677499
Clinical Medical Laboratory in Delray Beach, FL
NPI Status: Active since June 10, 2019
Contact Information
4733 W ATLANTIC AVE STE C16
DELRAY BEACH, FL
ZIP 33445
Phone: (561) 455-2162
Fax: (561) 354-5369
- Organization
- Clinical Medical Laboratory
- Accepts Insurance
About GENETICS INSTITUTE OF AMERICA LABORATORY FL1 CORP
This page provides the complete NPI Profile along with additional information for Genetics Institute Of America Laboratory Fl1 Corp, a provider established in Delray Beach, Florida operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1023677499 assigned on June 2019. The practitioner's primary taxonomy code is 291U00000X. The provider is registered as an organization and their NPI record was last updated 4 years ago. The authorized official of this NPI record is Holly Magliochetti (Ceo)
- NPI
- 1023677499
- Provider Name
- GENETICS INSTITUTE OF AMERICA LABORATORY FL1 CORP
- Entity Type
- Organization
- Location Address
- 4733 W ATLANTIC AVE STE C16 DELRAY BEACH, FL 33445
- Location Phone
- (561) 455-2162
- Location Fax
- (561) 354-5369
- Mailing Address
- 4733 W ATLANTIC AVE STE 12C DELRAY BEACH, FL 33445
- Mailing Phone
- (561) 475-3069
- Is Sole Proprietor?
- No
- Is Organization Subpart?
- No
- Enumeration Date
- 06-10-2019
- Last Update Date
- 05-17-2022
- Code Navigator
Establishments like Genetics Institute Of America Laboratory Fl1 Corp are healthcare facilities that may perform a wide range of laboratory procedures, assisted by doctors and medical technologists. Laboratories can be categorized according to their function as common diagnostic labs or specialty labs that conduct specialized or confirmatory tests. Different clinical laboratories could specialize in clinical chemistry, clinical microbiology, hematology, serology, clinical microscopy, cytopathology, molecular biology, or public health. Please inquire directly with this provider to confirm their test menu.
Location Map
Specialty - Primary Taxonomy
The NPI enumerator requires providers to submit at least one taxonomy code. A taxonomy code is a unique 10-character code that describes the healthcare provider type, classification, and the area of specialization. There could be only one primary taxonomy code per NPI record. For individual NPIs the license data is associated to the taxonomy code.
- Classification
Clinical Medical Laboratory
- Taxonomy Code
- 291U00000X
- Type
- Laboratories
- Taxonomy Description
- (1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.
Insurance Plans Accepted
According to publicly available information the provider might be accepting the following health plans from these health insurance companies:
- Blue Cross� Premier PPO Bronze Extra - PPO
- Blue Cross� Premier PPO Bronze Saver HSA - PPO
- Blue Cross� Premier PPO Bronze Secure - PPO
- Blue Cross� Premier PPO Gold - PPO
- Blue Cross� Premier PPO Gold Extra - PPO
- Blue Cross� Premier PPO Silver - PPO
- Blue Cross� Premier PPO Silver Extra - PPO
- Blue Cross� Premier PPO Silver Saver HSA - PPO
- Blue Cross� Premier PPO Value - PPO
*Please verify directly with this provider to make sure your insurance plan is currently accepted.
Areas of Expertise
The following services and procedures, recently provided to Medicare patients, illustrate the range of care this provider offers. This list reflects the variety of services available to all patients visiting the practice and is based on 2022 Medicare dataset. In general, the more frequently a provider treats specific conditions or performs particular procedures, the more experienced they become in addressing similar patient needs. The provider has delivered many of the services listed below to Medicare patients. Please note that this list does not include services provided to patients who are not covered by Medicare.
Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants
Gene analysis (adenomatous polyposis coli), full gene sequence
Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants
Gene analysis (catechol-o-methyltransferase) for c.472g>a (rs4680) variant
Gene analysis (coagulation factor v) leiden variant
Gene analysis (cytochrome p450 family 1, subfamily a, member 2) for common variants
Gene analysis (cytochrome p450 family 3 subfamily a member 4) for common variant
Gene analysis (cytochrome p450 family 3 subfamily a member 5) for common variant
Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants
Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants
Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants
Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis
Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis
Gene analysis (muts homolog 6 [e coli]) full sequence analysis
Gene analysis (partner and localizer of brca2) full sequence analysis
Gene analysis (phosphatase and tensin homolog), full sequence analysis
Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis
Gene analysis (prothrombin, coagulation factor ii) a variant
Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant
Gene analysis (tumor protein 53) full sequence analysis
Gene analysis (vitamin k epoxide reductase complex subunit 1) common variants
Molecular pathology procedure level 2
Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.
This service was performed 479 times for 479 patientsGene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.
This service was performed 384 times for 384 patientsGene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.
This service was performed 233 times for 233 patientsGene analysis for the c.472G>A (rs4680) variant involves studying a specific gene called catechol-O-methyltransferase (COMT). This test helps understand how your body processes certain chemicals that affect mood and pain. It's a simple, non-invasive procedure.
This service was performed 11 times for 11 patientsGene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.
This service was performed 478 times for 478 patientsGene analysis for Cytochrome P450 1A2 checks how your body processes medications. This test identifies common genetic variations that can affect your body's ability to metabolize certain drugs, helping your doctor personalize your treatment.
This service was performed 11 times for 11 patientsGene analysis for Cytochrome P450 3A4 checks how your body processes certain medications. This test identifies common variants in your genes that may affect drug response and dosage needs, helping to personalize your treatment.
This service was performed 16 times for 16 patientsGene analysis for the cytochrome P450 3A5 variant helps understand your body's response to certain medications. It's a genetic test that examines how your body metabolizes drugs, aiding in personalized medication plans.
This service was performed 18 times for 18 patientsGene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.
This service was performed 124 times for 124 patientsGene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.
This service was performed 145 times for 145 patientsGene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.
This service was performed 480 times for 480 patientsGene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.
This service was performed 79 times for 79 patientsGene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.
This service was performed 79 times for 79 patientsGene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.
This service was performed 79 times for 79 patientsGene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.
This service was performed 380 times for 380 patientsGene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.
This service was performed 378 times for 378 patientsGene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.
This service was performed 82 times for 82 patientsGene analysis for prothrombin (also known as coagulation factor II) is a test that examines your DNA to identify any variations in the prothrombin gene. These variations could potentially affect blood clotting, leading to an increased risk of certain health conditions.
This service was performed 478 times for 478 patientsGene analysis for the solute carrier organic anion transporter family, member 1b1 (SLCO1B1), common variant, is a test that examines your DNA to identify variations in the SLCO1B1 gene. This gene plays a crucial role in the body's ability to process certain medications.
This service was performed 176 times for 176 patientsGene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.
This service was performed 380 times for 380 patientsGene analysis of the vitamin K epoxide reductase complex subunit 1 common variants is a test that examines your DNA to identify potential variations in the VKORC1 gene. This gene influences how your body processes vitamin K, which plays a key role in blood clotting. This information can help tailor your healthcare to your unique genetic makeup.
This service was performed 16 times for 16 patientsA Molecular Pathology Procedure Level 2 is a laboratory test used to study genes at a molecular level. This helps identify genetic variations or mutations that may be associated with certain diseases or conditions. This information assists in diagnosing and managing your healthcare.
This service was performed 21 times for 21 patientsReviews for GENETICS INSTITUTE OF AMERICA LABORATORY FL1 CORP
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NPI NPI Number Validation
How NPI Validation Works
The NPI validation process uses the ISO-standard Luhn algorithm, a mathematical "handshake", to ensure that a provider's 10-digit ID is authentic and free of common typing errors.
To verify the NPI 1023677499, we treat the final digit (9) as the Check Digit—the target answer we need to reach. The process begins by taking the first nine digits and adding a constant value of 24, which accounts for the "80840" prefix required for all U.S. health identifiers. We then double every other digit starting from the right and sum the individual digits of those results together. For this specific NPI, that total comes to 61. The final step is to find the difference between that total and the next multiple of ten (70 - 61 = 9).
Digit-by-digit view
Use the first nine digits for the calculation. Starting from the right, double every other digit. The last digit is the check digit and is not part of the calculation.
Step 1: Double every other digit from the right
Starting with the rightmost digit of the first nine digits, double every other value. If doubling creates a two-digit number, add those digits together.
Step 2: Add all digits plus the NPI constant
Add the transformed values, the unchanged digits, and the constant 24.
Step 3: Find the amount needed to reach the next multiple of 10
The next multiple of ten after 61 is 70. The difference is the calculated check digit.
Frequently Asked Questions
The NPI number assigned to this healthcare provider is 1023677499, enumerated as an "organization" on June 10, 2019.
The provider is located at 4733 W ATLANTIC AVE STE C16 DELRAY BEACH, FL 33445 and the phone number is (561) 455-2162.
Clinical Medical Laboratory with taxonomy code 291U00000X.
The provider might be accepting Accepts: Blue Cross Blue Shield of Michigan Mutual. Please consult your insurance carrier or call the provider to verify.
