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rs121913154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913154(A;A)
Make rs121913154(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position7122658
GeneINSR
is asnp
is mentioned by
dbSNPrs121913154
ebirs121913154
HLIrs121913154
Exacrs121913154
Varsomers121913154
Maprs121913154
PheGenIrs121913154
hapmaprs121913154
1000 genomesrs121913154
hgdprs121913154
ensemblrs121913154
gopubmedrs121913154
geneviewrs121913154
scholarrs121913154
googlers121913154
pharmgkbrs121913154
gwascentralrs121913154
openSNPrs121913154
23andMers121913154
23andMe allrs121913154
SNP Nexus

SNPshotrs121913154
SNPdbers121913154
MSV3drs121913154
GWAS Ctlgrs121913154
Max Magnitude0
OMIM147670
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121913154(A;A)
Alt rs121913154(A;A)
Reference rs121913154(C;C)
Significance Pathogenic
Disease Insulin-resistant diabetes mellitus AND acanthosis nigricans
Variation info
Gene INSR
CLNDBN Insulin-resistant diabetes mellitus AND acanthosis nigricans
Reversed 1
HGVS NC_000019.9:g.7122669G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015819.28,