rs7955371

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(G;G)	0	common in clinvar

Make rs7955371(C;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

885321

Gene

WNK1

is a	snp
is	mentioned by
dbSNP	rs7955371
dbSNP (classic)	rs7955371
ClinGen	rs7955371
ebi	rs7955371
HLI	rs7955371
Exac	rs7955371
Gnomad	rs7955371
Varsome	rs7955371
LitVar	rs7955371
Map	rs7955371
PheGenI	rs7955371
Biobank	rs7955371
1000 genomes	rs7955371
hgdp	rs7955371
ensembl	rs7955371
geneview	rs7955371
scholar	rs7955371
google	rs7955371
pharmgkb	rs7955371
gwascentral	rs7955371
openSNP	rs7955371
23andMe	rs7955371
SNPshot	rs7955371
SNPdbe	rs7955371
MSV3d	rs7955371
GWAS Ctlg	rs7955371

GMAF

0.01056

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

ClinVar
Risk	Rs7955371(C;C)
Alt	Rs7955371(C;C)
Reference	Rs7955371(G;G)
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.994487G>C
CLNSRC
CLNACC	RCV000246878.1, RCV000263201.1, RCV000318455.1,