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rs121913157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913157(A;A)
Make rs121913157(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7120739
GeneINSR
is asnp
is mentioned by
dbSNPrs121913157
ClinGenrs121913157
ebirs121913157
HLIrs121913157
Exacrs121913157
Varsomers121913157
Maprs121913157
PheGenIrs121913157
hapmaprs121913157
1000 genomesrs121913157
hgdprs121913157
ensemblrs121913157
gopubmedrs121913157
geneviewrs121913157
scholarrs121913157
googlers121913157
pharmgkbrs121913157
gwascentralrs121913157
openSNPrs121913157
23andMers121913157
23andMe allrs121913157
SNP Nexus

SNPshotrs121913157
SNPdbers121913157
MSV3drs121913157
GWAS Ctlgrs121913157
Max Magnitude0
OMIM147670
Desc
Variant0031
Relatedalso
ClinVar
Risk rs121913157(A;A)
Alt rs121913157(A;A)
Reference Rs121913157(G;G)
Significance Pathogenic
Disease Insulin resistance
Variation info
Gene INSR
CLNDBN Insulin resistance
Reversed 1
HGVS NC_000019.9:g.7120750C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000015824.25,