Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909384

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909384(G;T)
Make rs121909384(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position56885328
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs121909384
ebirs121909384
HLIrs121909384
Exacrs121909384
Varsomers121909384
Maprs121909384
PheGenIrs121909384
hapmaprs121909384
1000 genomesrs121909384
hgdprs121909384
ensemblrs121909384
gopubmedrs121909384
geneviewrs121909384
scholarrs121909384
googlers121909384
pharmgkbrs121909384
gwascentralrs121909384
openSNPrs121909384
23andMers121909384
23andMe allrs121909384
SNP Nexus

SNPshotrs121909384
SNPdbers121909384
MSV3drs121909384
GWAS Ctlgrs121909384
Merged fromRs28936389
Max Magnitude0
OMIM600968
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909384(T;T)
Alt rs121909384(T;T)
Reference rs121909384(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56919240G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009125.2,