Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033591
rs111033591
Entrez Id: 65125
Gene Symbol: WNK1
WNK1
CUI: C1840391
Disease:
Pseudohypoaldosteronism, Type IIc
T 0.700 CausalMutation CLINVAR Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians. 15911806 2005