Gene: WNK1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033591
rs111033591
WNK1
T 0.700 CausalMutation CLINVAR Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians. 15911806

2005
dbSNP: rs137852735
rs137852735
WNK1
CA 0.700 CausalMutation CLINVAR Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates. 15060842

2004