rs371443644

Orientation

plus

Stabilized

plus

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

Make rs371443644(C;T)

Make rs371443644(T;T)

Reference

GRCh38 38.1/142

Chromosome

16

Position

56865414

Gene

SLC12A3

is a	snp
is	mentioned by
dbSNP	rs371443644
dbSNP (classic)	rs371443644
ClinGen	rs371443644
ebi	rs371443644
HLI	rs371443644
Exac	rs371443644
Gnomad	rs371443644
Varsome	rs371443644
LitVar	rs371443644
Map	rs371443644
PheGenI	rs371443644
Biobank	rs371443644
1000 genomes	rs371443644
hgdp	rs371443644
ensembl	rs371443644
geneview	rs371443644
scholar	rs371443644
google	rs371443644
pharmgkb	rs371443644
gwascentral	rs371443644
openSNP	rs371443644
23andMe	rs371443644
SNPshot	rs371443644
SNPdbe	rs371443644
MSV3d	rs371443644
GWAS Ctlg	rs371443644

Max Magnitude

0

ClinVar
Risk	rs371443644(T;T)
Alt	rs371443644(T;T)
Reference	Rs371443644(C;C)
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.56899326C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000087747.4, RCV000489628.1,