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rs121909381

From SNPedia

Merged intors121909380
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909381(G;T)
Make rs121909381(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position56886402
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs121909381
ebirs121909381
HLIrs121909381
Exacrs121909381
Varsomers121909381
Maprs121909381
PheGenIrs121909381
hapmaprs121909381
1000 genomesrs121909381
hgdprs121909381
ensemblrs121909381
gopubmedrs121909381
geneviewrs121909381
scholarrs121909381
googlers121909381
pharmgkbrs121909381
gwascentralrs121909381
openSNPrs121909381
23andMers121909381
23andMe allrs121909381
SNP Nexus

SNPshotrs121909381
SNPdbers121909381
MSV3drs121909381
GWAS Ctlgrs121909381
StatusMerged into rs121909380
Max Magnitude0
OMIM600968
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909381(T;T)
Alt rs121909381(T;T)
Reference rs121909381(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56920314G>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000029337.1,