rs886039753

Orientation

plus

Stabilized

plus

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

Make rs886039753(C;T)

Make rs886039753(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

56885288

Gene

SLC12A3

is a	snp
is	mentioned by
dbSNP	rs886039753
dbSNP (classic)	rs886039753
ClinGen	rs886039753
ebi	rs886039753
HLI	rs886039753
Exac	rs886039753
Gnomad	rs886039753
Varsome	rs886039753
LitVar	rs886039753
Map	rs886039753
PheGenI	rs886039753
Biobank	rs886039753
1000 genomes	rs886039753
hgdp	rs886039753
ensembl	rs886039753
geneview	rs886039753
scholar	rs886039753
google	rs886039753
pharmgkb	rs886039753
gwascentral	rs886039753
openSNP	rs886039753
23andMe	rs886039753
SNPshot	rs886039753
SNPdbe	rs886039753
MSV3d	rs886039753
GWAS Ctlg	rs886039753

Max Magnitude

0

ClinVar
Risk	rs886039753(T;T)
Alt	rs886039753(T;T)
Reference	Rs886039753(C;C)
Significance	Pathogenic
Disease	Familial hypokalemia-hypomagnesemia
Variation	info
Gene	SLC12A3
CLNDBN	Familial hypokalemia-hypomagnesemia
Reversed	0
HGVS	NC_000016.9:g.56919200C>T
CLNSRC
CLNACC	RCV000256196.1,