rs956868

Orientation

plus

Stabilized

plus

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

Make rs956868(A;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

881746

Gene

WNK1

is a	snp
is	mentioned by
dbSNP	rs956868
dbSNP (classic)	rs956868
ClinGen	rs956868
ebi	rs956868
HLI	rs956868
Exac	rs956868
Gnomad	rs956868
Varsome	rs956868
LitVar	rs956868
Map	rs956868
PheGenI	rs956868
Biobank	rs956868
1000 genomes	rs956868
hgdp	rs956868
ensembl	rs956868
geneview	rs956868
scholar	rs956868
google	rs956868
pharmgkb	rs956868
gwascentral	rs956868
openSNP	rs956868
23andMe	rs956868
SNPshot	rs956868
SNPdbe	rs956868
MSV3d	rs956868
GWAS Ctlg	rs956868

GMAF

0.1529

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 19347040] Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.

[PMID 19584173] Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.

ClinVar
Risk	Rs956868(C;C)
Alt	Rs956868(C;C)
Reference	Rs956868(A;A)
Significance	Non-pathogenic
Disease	not specified Hereditary sensory and autonomic neuropathy type II Pseudohypoaldosteronism
Variation	info
Gene	WNK1
CLNDBN	not specified Hereditary sensory and autonomic neuropathy type II Pseudohypoaldosteronism, type 2
Reversed	0
HGVS	NC_000012.11:g.990912A>C
CLNSRC
CLNACC	RCV000251124.1, RCV000332623.1, RCV000368653.1,