rs568513106

Orientation

plus

Stabilized

plus

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

Make rs568513106(C;C)

Make rs568513106(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

56870699

Gene

SLC12A3

is a	snp
is	mentioned by
dbSNP	rs568513106
dbSNP (classic)	rs568513106
ClinGen	rs568513106
ebi	rs568513106
HLI	rs568513106
Exac	rs568513106
Gnomad	rs568513106
Varsome	rs568513106
LitVar	rs568513106
Map	rs568513106
PheGenI	rs568513106
Biobank	rs568513106
1000 genomes	rs568513106
hgdp	rs568513106
ensembl	rs568513106
geneview	rs568513106
scholar	rs568513106
google	rs568513106
pharmgkb	rs568513106
gwascentral	rs568513106
openSNP	rs568513106
23andMe	rs568513106
SNPshot	rs568513106
SNPdbe	rs568513106
MSV3d	rs568513106
GWAS Ctlg	rs568513106

Max Magnitude

0

ClinVar
Risk	rs568513106(C;C)
Alt	rs568513106(C;C)
Reference	Rs568513106(T;T)
Significance	Probable-Pathogenic
Disease	Familial hypokalemia-hypomagnesemia
Variation	info
Gene	SLC12A3
CLNDBN	Familial hypokalemia-hypomagnesemia
Reversed	0
HGVS	NC_000016.9:g.56904611T>C
CLNSRC	Baylor College of Medicine
CLNACC	RCV000191129.1,