Variant: rs111033591 

    present in Gene: WNK1
    present in Chromosome: 12
    Position on Chromosome: 868697
    Alleles of this Variant: C/T

rs111033591 in WNK1 gene and Neuropathy, Hereditary Sensory And Autonomic, Type IIA PMID 15911806 2005 Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.

rs111033591 in WNK1 gene and Pseudohypoaldosteronism, Type IIc PMID 15911806 2005 Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.