rs387906332

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AG;AG)	0	common in clinvar
(GA;GA)	0	common in clinvar
(I;I)	0	common genotype

Make rs387906332(-;-)

Make rs387906332(-;GA)

Reference

GRCh38 38.1/141

Chromosome

12

Position

859435

Gene

WNK1

is a	snp
is	mentioned by
dbSNP	rs387906332
dbSNP (classic)	rs387906332
ClinGen	rs387906332
ebi	rs387906332
HLI	rs387906332
Exac	rs387906332
Gnomad	rs387906332
Varsome	rs387906332
LitVar	rs387906332
Map	rs387906332
PheGenI	rs387906332
Biobank	rs387906332
1000 genomes	rs387906332
hgdp	rs387906332
ensembl	rs387906332
geneview	rs387906332
scholar	rs387906332
google	rs387906332
pharmgkb	rs387906332
gwascentral	rs387906332
openSNP	rs387906332
23andMe	rs387906332
SNPshot	rs387906332
SNPdbe	rs387906332
MSV3d	rs387906332
GWAS Ctlg	rs387906332

Max Magnitude

0

ClinVar
Risk	rs387906332(-;-)
Alt	rs387906332(-;-)
Reference	Rs387906332(AG;AG)
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.968601_968602delGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005478.4,