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rs121434593

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434593(A;A)
Make rs121434593(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position40237979
GeneAKT2
is asnp
is mentioned by
dbSNPrs121434593
ebirs121434593
HLIrs121434593
Exacrs121434593
Varsomers121434593
Maprs121434593
PheGenIrs121434593
hapmaprs121434593
1000 genomesrs121434593
hgdprs121434593
ensemblrs121434593
gopubmedrs121434593
geneviewrs121434593
scholarrs121434593
googlers121434593
pharmgkbrs121434593
gwascentralrs121434593
openSNPrs121434593
23andMers121434593
23andMe allrs121434593
SNP Nexus

SNPshotrs121434593
SNPdbers121434593
MSV3drs121434593
GWAS Ctlgrs121434593
Max Magnitude0
OMIM164731
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434593(A;A)
Alt rs121434593(A;A)
Reference rs121434593(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene AKT2
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000019.9:g.40743886C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015016.25,