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Condition

Diabetes mellitus type 1
Synonyms: Diabetes Mellitus, Juvenile-Onset; Type I diabetes mellitus
Gene: IL6

Labs matching your search


9 labs with tests matching your search
Results:
36 genetic tests from 9 labs with tests matching your search
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Diabetes, susceptibility to, 222100, Autosomal recessive (IL6 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Diabetes mellitus, type I, susceptibility to, 222100, Autosomal recessive (FOXP3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Diabetes mellitus, insulin-dependent, 222100, Autosomal recessive (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Diabetes mellitus, insulin-dependent, 222100, Autosomal recessive (HNF1A gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Diabetes mellitus, type 1, susceptibility to, 222100, Autosomal recessive (OAS1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Diabetes, type 1, susceptibility to, 222100, Autosomal recessive (ITPR3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Diabetes, type 1, susceptibility to, 222100, Autosomal recessive (PTPN22 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
469448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GenepoweRx_Diabetes Care

GenepoweRx, Uppaluri K&H Personalized Medicine Clinic
India
1741
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Invitae Cholestasis Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
210134
  • D Deletion/duplication analysis

Invitae Hypoglycemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
173119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Monogenic Diabetes Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
5928
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Viral infection, susceptibility to (OAS1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Invitae Progressive Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
310195
  • D Deletion/duplication analysis

Monogenic Diabetes Panel

PreventionGenetics, part of Exact Sciences
United States
10154
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Glomerular Proteinuria NGS Panel

Fulgent Genetics
United States
18276
  • 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

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome (FOXP3 Single Gene Test)

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
36 tests from 9 labs
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Page 1 of 2
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
GenepoweRx_Diabetes Care by GenepoweRx, Uppaluri K&H Personalized Medicine Clinic
17 conditions, 41 genes
Invitae Cholestasis Panel by Labcorp Genetics (formerly Invitae), LabCorp
210 conditions, 134 genes
Invitae Hypoglycemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
173 conditions, 119 genes
Invitae Monogenic Diabetes Panel by Labcorp Genetics (formerly Invitae), LabCorp
59 conditions, 28 genes
Invitae Progressive Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
310 conditions, 195 genes
Monogenic Diabetes Panel by PreventionGenetics, part of Exact Sciences
101 conditions, 54 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.