Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033591
rs111033591
WNK1
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		T 0.700 CausalMutation CLINVAR Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians. 15911806

2005