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rs121913150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913150(A;A)
Make rs121913150(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7120707
GeneINSR
is asnp
is mentioned by
dbSNPrs121913150
ebirs121913150
HLIrs121913150
Exacrs121913150
Varsomers121913150
Maprs121913150
PheGenIrs121913150
hapmaprs121913150
1000 genomesrs121913150
hgdprs121913150
ensemblrs121913150
gopubmedrs121913150
geneviewrs121913150
scholarrs121913150
googlers121913150
pharmgkbrs121913150
gwascentralrs121913150
openSNPrs121913150
23andMers121913150
23andMe allrs121913150
SNP Nexus

SNPshotrs121913150
SNPdbers121913150
MSV3drs121913150
GWAS Ctlgrs121913150
Max Magnitude0
OMIM147670
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121913150(A;A)
Alt rs121913150(A;A)
Reference rs121913150(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene INSR
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000019.9:g.7120718C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015815.29,