rs779944215, ADCY10

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Teratozoospermia
CUI: C0403824
Disease: Teratozoospermia
0.700 CausalMutation CLINVAR ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. 31119281 2019
Asthenozoospermia
CUI: C0403823
Disease: Asthenozoospermia
0.700 CausalMutation CLINVAR ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. 31119281 2019