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rs121913142

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913142(G;G)
Make rs121913142(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position7172333
GeneINSR
is asnp
is mentioned by
dbSNPrs121913142
ebirs121913142
HLIrs121913142
Exacrs121913142
Varsomers121913142
Maprs121913142
PheGenIrs121913142
hapmaprs121913142
1000 genomesrs121913142
hgdprs121913142
ensemblrs121913142
gopubmedrs121913142
geneviewrs121913142
scholarrs121913142
googlers121913142
pharmgkbrs121913142
gwascentralrs121913142
openSNPrs121913142
23andMers121913142
23andMe allrs121913142
SNP Nexus

SNPshotrs121913142
SNPdbers121913142
MSV3drs121913142
GWAS Ctlgrs121913142
Max Magnitude0
OMIM147670
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121913142(G;G)
Alt rs121913142(G;G)
Reference rs121913142(T;T)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene INSR
CLNDBN Diabetes mellitus, insulin-resistant
Reversed 1
HGVS NC_000019.9:g.7172344A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015805.32,