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rs147901432

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147901432(A;A)
Make rs147901432(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position56885364
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs147901432
dbSNP (classic)rs147901432
ClinGenrs147901432
ebirs147901432
HLIrs147901432
Exacrs147901432
Gnomadrs147901432
Varsomers147901432
LitVarrs147901432
Maprs147901432
PheGenIrs147901432
Biobankrs147901432
1000 genomesrs147901432
hgdprs147901432
ensemblrs147901432
geneviewrs147901432
scholarrs147901432
googlers147901432
pharmgkbrs147901432
gwascentralrs147901432
openSNPrs147901432
23andMers147901432
23andMe allrs147901432
SNPshotrs147901432
SNPdbers147901432
MSV3drs147901432
GWAS Ctlgrs147901432
Max Magnitude0
ClinVar
Risk rs147901432(A;A)
Alt rs147901432(A;A)
Reference Rs147901432(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56919276G>A
CLNSRC Illumina
CLNACC RCV000362354.1,