Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1328641
rs1328641
SOHLH2 ; CCDC169-SOHLH2
0.010 GeneticVariation BEFREE The SNP rs1328641 might influence testes development in the NOA patients. 25463635

2015