Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113993959
rs113993959
T 0.700 CausalMutation CLINVAR

dbSNP: rs74597325
rs74597325
T 0.700 CausalMutation CLINVAR

dbSNP: rs78655421
rs78655421
0.010 GeneticVariation BEFREE For those with chest HRCT results available, 75% p.Arg117His-5TCF, 33% p.Arg117His-7TCF and 27% p.Arg117His-7TCFTR patients had bronchiectasis. 30279124

2019