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rs121918407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918407(C;C)
Make rs121918407(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position156579109
GeneGPD2
is asnp
is mentioned by
dbSNPrs121918407
ebirs121918407
HLIrs121918407
Exacrs121918407
Varsomers121918407
Maprs121918407
PheGenIrs121918407
hapmaprs121918407
1000 genomesrs121918407
hgdprs121918407
ensemblrs121918407
gopubmedrs121918407
geneviewrs121918407
scholarrs121918407
googlers121918407
pharmgkbrs121918407
gwascentralrs121918407
openSNPrs121918407
23andMers121918407
23andMe allrs121918407
SNP Nexus

SNPshotrs121918407
SNPdbers121918407
MSV3drs121918407
GWAS Ctlgrs121918407
Max Magnitude0
OMIM138430
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918407(C;C)
Alt rs121918407(C;C)
Reference rs121918407(T;T)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene GPD2
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000002.11:g.157435621T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017461.27,