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rs387906332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs387906332(-;-)
Make rs387906332(-;GA)
ReferenceGRCh38 38.1/141
Chromosome12
Position859435
GeneWNK1
is asnp
is mentioned by
dbSNPrs387906332
ebirs387906332
HLIrs387906332
Exacrs387906332
Varsomers387906332
Maprs387906332
PheGenIrs387906332
hapmaprs387906332
1000 genomesrs387906332
hgdprs387906332
ensemblrs387906332
gopubmedrs387906332
geneviewrs387906332
scholarrs387906332
googlers387906332
pharmgkbrs387906332
gwascentralrs387906332
openSNPrs387906332
23andMers387906332
23andMe allrs387906332
SNP Nexus

SNPshotrs387906332
SNPdbers387906332
MSV3drs387906332
GWAS Ctlgrs387906332
Max Magnitude0
ClinVar
Risk rs387906332(;)
Alt rs387906332(;)
Reference rs387906332(AG;AG)
Significance Pathogenic
Disease Neuropathy
Variation info
Gene WNK1
CLNDBN Neuropathy, hereditary sensory, type II
Reversed 0
HGVS NC_000012.11:g.968601_968602delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005478.3,