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rs886041108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position56879544
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs886041108
dbSNP (classic)rs886041108
ClinGenrs886041108
ebirs886041108
HLIrs886041108
Exacrs886041108
Gnomadrs886041108
Varsomers886041108
LitVarrs886041108
Maprs886041108
PheGenIrs886041108
Biobankrs886041108
1000 genomesrs886041108
hgdprs886041108
ensemblrs886041108
geneviewrs886041108
scholarrs886041108
googlers886041108
pharmgkbrs886041108
gwascentralrs886041108
openSNPrs886041108
23andMers886041108
23andMe allrs886041108
SNPshotrs886041108
SNPdbers886041108
MSV3drs886041108
GWAS Ctlgrs886041108
Max Magnitude0
ClinVar
Risk rs886041108(-;-)
Alt rs886041108(-;-)
Reference Rs886041108(C;C)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56913456delC
CLNSRC
CLNACC RCV000258950.1,