Annotation Detail
Information
- Associated Genes
- IGF2BP2
- Associated Variants
-
IGF2BP2 c.239+29254C>A
(
ENST00000346192.7,
ENST00000382199.7,
ENST00000421047.3,
ENST00000457616.6 )
IGF2BP2 c.239+29254C>A ( ENST00000346192.7, ENST00000382199.7, ENST00000421047.3, ENST00000457616.6 ) - Associated Disease
- Diabetes mellitus type 2, susceptibility to
- Source Database
- ClinVar
- Description
- NM_006548.6(IGF2BP2):c.239+29254C>A AND Diabetes mellitus type 2, susceptibility to
- ClinVar Allele ID
- 17474
- ClinVar RefSeq Alternation Syntax
- NM_001007225.3:c.239+29254C>A
- ClinVar RefSeq Alternation Syntax
- NM_006548.6:c.239+29254C>A
- ClinVar RefSeq Alternation Syntax
- NM_001291873.3:c.50+27113C>A
- ClinVar RefSeq Alternation Syntax
- NM_001291872.3:c.50+27113C>A
- ClinVar RefSeq Alternation Syntax
- NM_001291874.3:c.50+27113C>A
- ClinVar RefSeq Alternation Syntax
- NM_001291869.3:c.239+29254C>A
- ClinVar RefSeq Alternation Syntax
- NM_001291875.3:c.-106+27113C>A
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2007-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000002537
- ClinVar Disease
- Diabetes mellitus type 2, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 17463249
- Pubmed
- 17463246
- Pubmed
- 17463248
Drugs