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rs111033592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033592(C;T)
Make rs111033592(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position868046
GeneWNK1
is asnp
is mentioned by
dbSNPrs111033592
ebirs111033592
HLIrs111033592
Exacrs111033592
Varsomers111033592
Maprs111033592
PheGenIrs111033592
hapmaprs111033592
1000 genomesrs111033592
hgdprs111033592
ensemblrs111033592
gopubmedrs111033592
geneviewrs111033592
scholarrs111033592
googlers111033592
pharmgkbrs111033592
gwascentralrs111033592
openSNPrs111033592
23andMers111033592
23andMe allrs111033592
SNP Nexus

SNPshotrs111033592
SNPdbers111033592
MSV3drs111033592
GWAS Ctlgrs111033592
Max Magnitude0
OMIM605232
Desc
Variant0007
Relatedalso
OMIM605232
Desc
Variant0009
Relatedalso
ClinVar
Risk rs111033592(T;T)
Alt rs111033592(T;T)
Reference rs111033592(C;C)
Significance Pathogenic
Disease Neuropathy
Variation info
Gene WNK1
CLNDBN Neuropathy, hereditary sensory, type II
Reversed 0
HGVS NC_000012.11:g.977212C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005471.2,