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rs137852734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852734(-;-)
Make rs137852734(-;A)
ReferenceGRCh38 38.1/141
Chromosome12
Position868423
GeneWNK1
is asnp
is mentioned by
dbSNPrs137852734
ebirs137852734
HLIrs137852734
Exacrs137852734
Varsomers137852734
Maprs137852734
PheGenIrs137852734
hapmaprs137852734
1000 genomesrs137852734
hgdprs137852734
ensemblrs137852734
gopubmedrs137852734
geneviewrs137852734
scholarrs137852734
googlers137852734
pharmgkbrs137852734
gwascentralrs137852734
openSNPrs137852734
23andMers137852734
23andMe allrs137852734
SNP Nexus

SNPshotrs137852734
SNPdbers137852734
MSV3drs137852734
GWAS Ctlgrs137852734
Max Magnitude0
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,