Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893642

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893642(C;G)
Make rs104893642(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position226796916
GeneIRS1
is asnp
is mentioned by
dbSNPrs104893642
ebirs104893642
HLIrs104893642
Exacrs104893642
Varsomers104893642
Maprs104893642
PheGenIrs104893642
hapmaprs104893642
1000 genomesrs104893642
hgdprs104893642
ensemblrs104893642
gopubmedrs104893642
geneviewrs104893642
scholarrs104893642
googlers104893642
pharmgkbrs104893642
gwascentralrs104893642
openSNPrs104893642
23andMers104893642
23andMe allrs104893642
SNP Nexus

SNPshotrs104893642
SNPdbers104893642
MSV3drs104893642
GWAS Ctlgrs104893642
Max Magnitude0
ClinVar
Risk rs104893642(G,T;G,T)
Alt rs104893642(G,T;G,T)
Reference rs104893642(C;C)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene IRS1
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000002.11:g.227661632G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022626.25,