Annotation Detail
Information
- Associated Genes
- IRS2
- Associated Variants
-
IRS2 p.Gly1057Asp (p.G1057D)
(
ENST00000375856.5 )
IRS2 p.Gly1057Asp (p.G1057D) ( ENST00000375856.5 ) - Associated Disease
- DIABETES, TYPE II, SUSCEPTIBILITY TO
- Source Database
- ClinVar
- Description
- NM_003749.3(IRS2):c.3170G>A (p.Gly1057Asp) AND DIABETES, TYPE II, SUSCEPTIBILITY TO
- ClinVar Allele ID
- 23859
- ClinVar RefSeq Alternation Syntax
- NM_003749.3:c.3170G>A
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2001-10-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000009368
- ClinVar Disease
- DIABETES, TYPE II, SUSCEPTIBILITY TO
- Observed Origin Sample
- germline
- Pubmed
- 11030756
- Pubmed
- 11600548
Drugs