rs371195126, SEPTIN12

N. diseases: 3
Disease: Asthenozoospermia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Asthenozoospermia
CUI: C0403823
Disease: Asthenozoospermia
0.010 GeneticVariation BEFREE The patient carrying SEPT12(D197N) presented with oligoasthenozoospermia, whereas the SEPT12(T89M) patient had asthenoteratozoospermia. 22275165 2012