PATHWAY DIAGNOSTIC LABORATORIES, LLC
NPI 1952143612
Clinical Medical Laboratory in New Braunfels, TX

Q: What is Pathway Diagnostic Laboratories, LLC's NPI number?

The NPI number for Pathway Diagnostic Laboratories, LLC is 1952143612. It was assigned to this organization in the NPPES registry on June 12, 2024.

Q: What is Pathway Diagnostic Laboratories, LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

Active since June 12, 2024

910 GRUENE RD BLDG 5A, NEW BRAUNFELS, TX 78130(830) 327-8393 Get Directions Write a Review

NPPES record last updated: July 7, 2024. Verified against the NPPES registry weekly; last sync: November 08, 2026.

Record update history: Jul 7, 2024, Jun 12, 2024 (2 updates tracked since 2024).

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About Pathway Diagnostic Laboratories, Llc NPPES

Official registry information on file with the National Plan and Provider Enumeration System.

PATHWAY DIAGNOSTIC LABORATORIES, LLC (NPI 1952143612) is a healthcare organization registered as a clinical medical laboratory in New Braunfels, Texas and active in the NPI registry since June 2024. The organization lists Tavane Ragan, Chief Executive Officer, as its authorized official.

NPPES Registry Identity

NPI1952143612

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NamePATHWAY DIAGNOSTIC LABORATORIES, LLC

Location Address910 GRUENE RD BLDG 5ANew Braunfels, TX 78130-0200

Mailing Address910 Gruene Rd Bldg 5aNew Braunfels, TX 78130-0200 · (830) 327-8393

Phone(830) 327-8393

Organization SubpartNo

Authorized OfficialTavane RaganChief Executive Officer · (830) 327-8393

Enumeration DateJune 12, 2024

Last NPPES UpdateJuly 7, 20242 updates tracked since enumeration

NPPES CertifiedJuly 7, 2024

✔ NPI 1952143612 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

Definition

(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.

910 GRUENE RD BLDG 5A, New Braunfels, TX 78130

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Accepted Insurance

The full list of accepted plans is on the Insurance tab. Issuers include Blue Cross and Blue Shield of Texas.Insurance ›

Areas of Expertise CMS Part B claims 26

Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.

Gene analysis (coagulation factor ix) full sequence analysis 81238

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

165 services138 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence 81223

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

161 services150 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

144 services128 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295

Gene 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.

136 services136 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis 81298

Gene 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.

134 services134 patients

Gene analysis (partner and localizer of brca2) full sequence analysis 81307

Gene 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.

134 services134 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis 81317

Gene 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.

134 services134 patients

Gene analysis (janus kinase 2) targeted sequence analysis 81279

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

133 services133 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 81339

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

133 services133 patients

Gene analysis (bloom syndrome, recq helicase-like) 81209

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

131 services131 patients

Gene analysis (fanconi anemia, complementation group c) common variant 81242

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

131 services131 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

131 services131 patients

Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants 81330

Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.

93 services93 patients

Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants 81332

Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.

93 services93 patients

Gene analysis (methyl cpg binding protein 2) full sequence analysis 81302

Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.

89 services88 patients

Gene analysis (transforming growth factor beta-induced) for common variants 81333

Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.

63 services61 patients

Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence 81185

Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.

50 services50 patients

Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes 81443

This procedure involves analyzing your genetic material to identify specific mutations that could cause severe inherited conditions. It examines 15 or more genes. The information can help in diagnosis, treatment planning, and understanding your risk for certain diseases.

35 services35 patients

Gene analysis (retinal disorders), genomic sequence 81434

Gene analysis for retinal disorders is a process where your DNA is examined to identify any changes or mutations that may be causing or could lead to vision problems. It's like reading a book to find any spelling mistakes that could alter the story.

33 services33 patients

Gene analysis (gap junction protein, beta 6, 30kda, connexin 30), common variants 81254

Gene analysis for Connexin 30 involves studying your DNA to identify variations in the GJB6 gene. This gene helps produce a protein vital for cell communication. Detecting common variants can help understand certain health conditions.

31 services31 patients

Gene analysis (cystatin b) of full sequence 81189

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

23 services23 patients

Gene analysis (hemochromatosis) common variants 81256

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

23 services23 patients

Gene analysis panel for evaluation of genes associated with epilepsy 81419

A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.

22 services22 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291

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.

19 services19 patients

Test for detecting genes 81440

A gene detection test is a medical procedure that identifies specific genes in your DNA. It helps to understand your genetic makeup and potential health risks. The process involves taking a small sample of your body tissue, like blood or saliva, which is then analyzed in a lab.

16 services16 patients

Gene analysis panel for hereditary disorders of the peripheral nervous system 81448

A gene analysis panel for hereditary disorders of the peripheral nervous system is a test that checks for genetic mutations linked to certain nerve disorders. It helps identify if you have a higher risk of developing these conditions.

16 services16 patients

Frequently Asked Questions NPPES & CMS

Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.

What is Pathway Diagnostic Laboratories, LLC's NPI number?

The NPI number for Pathway Diagnostic Laboratories, LLC is 1952143612. It was assigned to this organization in the NPPES registry on June 12, 2024.

Where is Pathway Diagnostic Laboratories, LLC located?

Pathway Diagnostic Laboratories, LLC is located at 910 Gruene Rd Bldg 5A, New Braunfels, TX 78130. The listed phone number is (830) 327-8393.

What is Pathway Diagnostic Laboratories, LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

What insurance does Pathway Diagnostic Laboratories, LLC accept?

Health plans from Blue Cross and Blue Shield of Texas list Pathway Diagnostic Laboratories, LLC as in-network in at least one marketplace plan. Coverage varies by plan and year; verify with the insurer or the provider before a visit.

When was this NPI record last updated?

The NPPES record for Pathway Diagnostic Laboratories, LLC was last updated on July 7, 2024. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 2 years ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.