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rs12708965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs12708965(C;T)
Make rs12708965(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position56902407
GeneMIR6863, SLC12A3
is asnp
is mentioned by
dbSNPrs12708965
dbSNP (classic)rs12708965
ClinGenrs12708965
ebirs12708965
HLIrs12708965
Exacrs12708965
Gnomadrs12708965
Varsomers12708965
LitVarrs12708965
Maprs12708965
PheGenIrs12708965
Biobankrs12708965
1000 genomesrs12708965
hgdprs12708965
ensemblrs12708965
geneviewrs12708965
scholarrs12708965
googlers12708965
pharmgkbrs12708965
gwascentralrs12708965
openSNPrs12708965
23andMers12708965
23andMe allrs12708965
SNPshotrs12708965
SNPdbers12708965
MSV3drs12708965
GWAS Ctlgrs12708965
GMAF0.03673
Max Magnitude0
? (C;C) (C;T) (T;T) 28




ClinVar
Risk rs12708965(T;T)
Alt rs12708965(T;T)
Reference Rs12708965(C;C)
Significance Probable-non-pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3 MIR6863
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56936319C>T
CLNSRC
CLNACC RCV000405253.1,