rs12828016

Orientation

plus

Stabilized

plus

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

Make rs12828016(G;T)

Make rs12828016(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

889199

Gene

WNK1

is a	snp
is	mentioned by
dbSNP	rs12828016
dbSNP (classic)	rs12828016
ClinGen	rs12828016
ebi	rs12828016
HLI	rs12828016
Exac	rs12828016
Gnomad	rs12828016
Varsome	rs12828016
LitVar	rs12828016
Map	rs12828016
PheGenI	rs12828016
Biobank	rs12828016
1000 genomes	rs12828016
hgdp	rs12828016
ensembl	rs12828016
geneview	rs12828016
scholar	rs12828016
google	rs12828016
pharmgkb	rs12828016
gwascentral	rs12828016
openSNP	rs12828016
23andMe	rs12828016
SNPshot	rs12828016
SNPdbe	rs12828016
MSV3d	rs12828016
GWAS Ctlg	rs12828016

GMAF

0.3861

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

[PMID 23059770] Common Variation in With No-Lysine Kinase 1 (WNK1) and Blood Pressure Responses to Dietary Sodium or Potassium Interventions

ClinVar
Risk	rs12828016(T;T)
Alt	rs12828016(T;T)
Reference	Rs12828016(G;G)
Significance	Non-pathogenic
Disease	not specified Pseudohypoaldosteronism Hereditary sensory and autonomic neuropathy type II
Variation	info
Gene	WNK1
CLNDBN	not specified Pseudohypoaldosteronism, type 2 Hereditary sensory and autonomic neuropathy type II
Reversed	0
HGVS	NC_000012.11:g.998365G>T
CLNSRC
CLNACC	RCV000250212.1, RCV000355246.1, RCV000394062.1,