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rs387906331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906331(-;-)
Make rs387906331(-;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position868470
GeneWNK1
is asnp
is mentioned by
dbSNPrs387906331
ebirs387906331
HLIrs387906331
Exacrs387906331
Varsomers387906331
Maprs387906331
PheGenIrs387906331
hapmaprs387906331
1000 genomesrs387906331
hgdprs387906331
ensemblrs387906331
gopubmedrs387906331
geneviewrs387906331
scholarrs387906331
googlers387906331
pharmgkbrs387906331
gwascentralrs387906331
openSNPrs387906331
23andMers387906331
23andMe allrs387906331
SNP Nexus

SNPshotrs387906331
SNPdbers387906331
MSV3drs387906331
GWAS Ctlgrs387906331
Max Magnitude0
ClinVar
Risk rs387906331(;)
Alt rs387906331(;)
Reference rs387906331(G;G)
Significance Pathogenic
Disease Neuropathy
Variation info
Gene WNK1
CLNDBN Neuropathy, hereditary sensory, type II
Reversed 0
HGVS NC_000012.11:g.977636delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005477.4,