Gene: SCNN1A ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5742912
rs5742912
SCNN1A ; LOC107984500
0.010 GeneticVariation BEFREE Frequency of p.W493R was lower in CF parents than in Caucasian control subjects. 21917531

2012