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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Polyglandular autoimmune syndrome, type 1
Synonyms: APS I; AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA; Autoimmune polyendocrine syndrome type 1; Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia; Autoimmune polyendocrinopathy syndrome, type I; HYPOADRENOCORTICISM WITH HYPOPARATHYROIDISM AND SUPERFICIAL MONILIASIS; PGA I; Whitaker syndrome
Gene: AIRE
Results:
59 genetic tests from 21 labs with tests matching your search, 2 labs matching in other ways
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Download data for all or selected tests, using the check boxes in the search results to make your selection.
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Inborn Errors of Immunity and Cytopenias Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
754562
  • D Deletion/duplication analysis

Invitae Primary Immunodeficiency Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
552424
  • D Deletion/duplication analysis

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autoinflammatory Gene Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
182117
  • C Sequence analysis of the entire coding region

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
325300
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Partner Reflex to GeneSeq

Integrated Genetics Westborough, LabCorp
United States
330746
  • C Sequence analysis of the entire coding region

Horizon 274

Natera, Inc.
United States
265274
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 274 Plus TSE

Natera, Inc.
United States
265274
  • E Enzyme assay
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 274

Natera, Inc.
United States
265274
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Inborn Errors of Immunity GenePanel

Mayo Clinic Laboratories, Mayo Clinic
United States
374386
  • C Sequence analysis of the entire coding region

Targeted Variant, Fetal Analysis

Integrated Genetics Westborough, LabCorp
United States
292746
  • T Targeted variant analysis

GeneSeq PLUS, Fetal Analysis

Integrated Genetics Westborough, LabCorp
United States
292597
  • C Sequence analysis of the entire coding region

Targeted Variant Analysis

Integrated Genetics Westborough, LabCorp
United States
287578
  • T Targeted variant analysis

GeneSeq PLUS

Integrated Genetics Westborough, LabCorp
United States
287578
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Inheritest 500 PLUS Panel

Integrated Genetics Westborough, LabCorp
United States
287578
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
59 tests from 21 labs
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❮Page 1 of 3❯
Clinical Exome by Fulgent Genetics
5127 conditions, 4672 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
Invitae Primary Immunodeficiency Panel by Labcorp Genetics (formerly Invitae), LabCorp
552 conditions, 424 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
Comprehensive Primary Immunodeficiency NGS Panel by Fulgent Genetics
1048 conditions, 472 genes
Autoinflammatory Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
182 conditions, 117 genes
qCarrier Plus by Quantitative Genomic Medicine Laboratories, SL
325 conditions, 300 genes
Beacon Expanded Male Carrier Screening Panel by Fulgent Genetics
636 conditions, 298 genes
Partner Reflex to GeneSeq by Integrated Genetics Westborough, LabCorp
330 conditions, 746 genes
Horizon 274 by Natera, Inc.
265 conditions, 274 genes
Horizon 274 Plus TSE by Natera, Inc.
265 conditions, 274 genes
Horizon 274 by Natera, Inc.
265 conditions, 274 genes
Inborn Errors of Immunity GenePanel by Mayo Clinic Laboratories, Mayo Clinic
374 conditions, 386 genes
Targeted Variant, Fetal Analysis by Integrated Genetics Westborough, LabCorp
292 conditions, 746 genes
GeneSeq PLUS, Fetal Analysis by Integrated Genetics Westborough, LabCorp
292 conditions, 597 genes
Targeted Variant Analysis by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes
GeneSeq PLUS by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes
Inheritest 500 PLUS Panel by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.