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rs121913146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913146(A;A)
Make rs121913146(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7267518
GeneINSR
is asnp
is mentioned by
dbSNPrs121913146
ebirs121913146
HLIrs121913146
Exacrs121913146
Varsomers121913146
Maprs121913146
PheGenIrs121913146
hapmaprs121913146
1000 genomesrs121913146
hgdprs121913146
ensemblrs121913146
gopubmedrs121913146
geneviewrs121913146
scholarrs121913146
googlers121913146
pharmgkbrs121913146
gwascentralrs121913146
openSNPrs121913146
23andMers121913146
23andMe allrs121913146
SNP Nexus

SNPshotrs121913146
SNPdbers121913146
MSV3drs121913146
GWAS Ctlgrs121913146
Max Magnitude0
OMIM147670
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121913146(A;A)
Alt rs121913146(A;A)
Reference rs121913146(G;G)
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.7267529C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015809.28,