rs78655421, CFTR

N. diseases: 17
Disease: Non-obstructive azoospermia ×
Source: BEFREE ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Non-obstructive azoospermia
CUI: C4021107
Disease: Non-obstructive azoospermia
0.010 GeneticVariation BEFREE In conclusion, the polyvariant mutant genes of CFTR: T5 allele and TG12-T5-V470 genotype are correlated with NOA, but F508del and R117H mutations have low possibility to be associated with NOA. 28456595 2017