Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397508638
rs397508638
CFTR
0.010 GeneticVariation BEFREE An Egyptian infant with the common CFTR mutation N1303K in exon 21 developed alkalosis, electrolyte disturbance, and pancreas insufficiency. 15357568

2004
dbSNP: rs80034486
rs80034486
CFTR
0.010 GeneticVariation BEFREE An Egyptian infant with the common CFTR mutation N1303K in exon 21 developed alkalosis, electrolyte disturbance, and pancreas insufficiency. 15357568

2004