rs2656927, UHRF1;ARRDC5

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Oligospermia
CUI: C0028960
Disease: Oligospermia
0.010 GeneticVariation BEFREE Interestingly, the genotype frequencies of SNP rs2656927 (P = 0.014) and rs8103849 (P < 0.001) significantly differed between men with oligozoospermia in case group 1 and normozoospermic men. 31802345 2019