rs121909379

Orientation

plus

Stabilized

plus

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

Make rs121909379(C;C)

Make rs121909379(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

56894558

Gene

SLC12A3

is a	snp
is	mentioned by
dbSNP	rs121909379
dbSNP (classic)	rs121909379
ClinGen	rs121909379
ebi	rs121909379
HLI	rs121909379
Exac	rs121909379
Gnomad	rs121909379
Varsome	rs121909379
LitVar	rs121909379
Map	rs121909379
PheGenI	rs121909379
Biobank	rs121909379
1000 genomes	rs121909379
hgdp	rs121909379
ensembl	rs121909379
geneview	rs121909379
scholar	rs121909379
google	rs121909379
pharmgkb	rs121909379
gwascentral	rs121909379
openSNP	rs121909379
23andMe	rs121909379
SNPshot	rs121909379
SNPdbe	rs121909379
MSV3d	rs121909379
GWAS Ctlg	rs121909379

Max Magnitude

0

OMIM	600968
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909379(C;C)
Alt	rs121909379(C;C)
Reference	Rs121909379(T;T)
Significance	Other
Disease	Familial hypokalemia-hypomagnesemia
Variation	info
Gene	SLC12A3
CLNDBN	Familial hypokalemia-hypomagnesemia
Reversed	0
HGVS	NC_000016.9:g.56928470T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009115.2,