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rs374163823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374163823(A;A)
Make rs374163823(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56879593
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs374163823
dbSNP (classic)rs374163823
ClinGenrs374163823
ebirs374163823
HLIrs374163823
Exacrs374163823
Gnomadrs374163823
Varsomers374163823
LitVarrs374163823
Maprs374163823
PheGenIrs374163823
Biobankrs374163823
1000 genomesrs374163823
hgdprs374163823
ensemblrs374163823
geneviewrs374163823
scholarrs374163823
googlers374163823
pharmgkbrs374163823
gwascentralrs374163823
openSNPrs374163823
23andMers374163823
23andMe allrs374163823
SNPshotrs374163823
SNPdbers374163823
MSV3drs374163823
GWAS Ctlgrs374163823
Max Magnitude0
ClinVar
Risk rs374163823(A;A)
Alt rs374163823(A;A)
Reference Rs374163823(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia not provided
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia not provided
Reversed 0
HGVS NC_000016.9:g.56913505G>A
CLNSRC
CLNACC RCV000286818.1, RCV000414425.1,