rs111033591, WNK1

N. diseases: 2
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neuropathy, Hereditary Sensory And Autonomic, Type IIA
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
0.700 CausalMutation CLINVAR Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians. 15911806 2005