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rs121909741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909741(A;A)
Make rs121909741(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position171007171
GeneSLC2A2
is asnp
is mentioned by
dbSNPrs121909741
ebirs121909741
HLIrs121909741
Exacrs121909741
Varsomers121909741
Maprs121909741
PheGenIrs121909741
hapmaprs121909741
1000 genomesrs121909741
hgdprs121909741
ensemblrs121909741
gopubmedrs121909741
geneviewrs121909741
scholarrs121909741
googlers121909741
pharmgkbrs121909741
gwascentralrs121909741
openSNPrs121909741
23andMers121909741
23andMe allrs121909741
SNP Nexus

SNPshotrs121909741
SNPdbers121909741
MSV3drs121909741
GWAS Ctlgrs121909741
Max Magnitude0
OMIM138160
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909741(A;A)
Alt rs121909741(A;A)
Reference rs121909741(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene SLC2A2
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000003.11:g.170724960C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017470.27,