rs147901432

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs147901432(A;A)

Make rs147901432(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

56885364

Gene

SLC12A3

is a	snp
is	mentioned by
dbSNP	rs147901432
dbSNP (classic)	rs147901432
ClinGen	rs147901432
ebi	rs147901432
HLI	rs147901432
Exac	rs147901432
Gnomad	rs147901432
Varsome	rs147901432
LitVar	rs147901432
Map	rs147901432
PheGenI	rs147901432
Biobank	rs147901432
1000 genomes	rs147901432
hgdp	rs147901432
ensembl	rs147901432
geneview	rs147901432
scholar	rs147901432
google	rs147901432
pharmgkb	rs147901432
gwascentral	rs147901432
openSNP	rs147901432
23andMe	rs147901432
SNPshot	rs147901432
SNPdbe	rs147901432
MSV3d	rs147901432
GWAS Ctlg	rs147901432

Max Magnitude

0

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,