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rs121909379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909379(C;C)
Make rs121909379(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position56894558
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs121909379
ebirs121909379
HLIrs121909379
Exacrs121909379
Varsomers121909379
Maprs121909379
PheGenIrs121909379
hapmaprs121909379
1000 genomesrs121909379
hgdprs121909379
ensemblrs121909379
gopubmedrs121909379
geneviewrs121909379
scholarrs121909379
googlers121909379
pharmgkbrs121909379
gwascentralrs121909379
openSNPrs121909379
23andMers121909379
23andMe allrs121909379
SNP Nexus

SNPshotrs121909379
SNPdbers121909379
MSV3drs121909379
GWAS Ctlgrs121909379
Max Magnitude0
OMIM600968
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909379(C;C)
Alt rs121909379(C;C)
Reference rs121909379(T;T)
Significance Other
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56928470T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009115.2,