Annotation Detail
Information
- Associated Genes
- INS INS-IGF2
- Associated Variants
-
INS p.Tyr108Cys (p.Y108C), INS-IGF2 c.187+923A>G
(
ENST00000250971.7,
ENST00000397270.1,
ENST00000381330.5,
ENST00000397262.5,
ENST00000512523.1 )
INS p.Tyr108Cys (p.Y108C), INS-IGF2 c.187+923A>G ( ENST00000250971.7, ENST00000381330.5, ENST00000397262.5, ENST00000512523.1, ENST00000397270.1 ) - Associated Disease
- Diabetes mellitus, permanent neonatal 4
- Source Database
- ClinVar
- Description
- NM_000207.3(INS):c.323A>G (p.Tyr108Cys) AND Diabetes mellitus, permanent neonatal 4
- ClinVar Allele ID
- 33972
- ClinVar RefSeq Alternation Syntax
- NM_001042376.3:c.187+923A>G
- ClinVar RefSeq Alternation Syntax
- NM_001291897.2:c.323A>G
- ClinVar RefSeq Alternation Syntax
- NM_000207.3:c.323A>G
- ClinVar RefSeq Alternation Syntax
- NM_001185098.2:c.323A>G
- ClinVar RefSeq Alternation Syntax
- NM_001185097.2:c.323A>G
- Clinical Significance Description
- Likely risk allele
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003389036
- ClinVar Disease
- Diabetes mellitus, permanent neonatal 4
- Observed Origin Sample
- unknown
Drugs