rs137852734

Orientation

plus

Stabilized

plus

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

Make rs137852734(-;-)

Make rs137852734(-;A)

Reference

GRCh38 38.1/141

Chromosome

12

Position

868423

Gene

WNK1

is a	snp
is	mentioned by
dbSNP	rs137852734
dbSNP (classic)	rs137852734
ClinGen	rs137852734
ebi	rs137852734
HLI	rs137852734
Exac	rs137852734
Gnomad	rs137852734
Varsome	rs137852734
LitVar	rs137852734
Map	rs137852734
PheGenI	rs137852734
Biobank	rs137852734
1000 genomes	rs137852734
hgdp	rs137852734
ensembl	rs137852734
geneview	rs137852734
scholar	rs137852734
google	rs137852734
pharmgkb	rs137852734
gwascentral	rs137852734
openSNP	rs137852734
23andMe	rs137852734
SNPshot	rs137852734
SNPdbe	rs137852734
MSV3d	rs137852734
GWAS Ctlg	rs137852734

Max Magnitude

0

ClinVar
Risk	rs137852734(-;-)
Alt	rs137852734(-;-)
Reference	Rs137852734(A;A)
Significance	Pathogenic
Disease	Hereditary sensory and autonomic neuropathy type IIA
Variation	info
Gene	WNK1
CLNDBN	Hereditary sensory and autonomic neuropathy type IIA
Reversed	0
HGVS	NC_000012.11:g.977589delA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020431.1,