Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555472691
rs1555472691
MEIOB
CUI: C4540179
Disease: SPERMATOGENIC FAILURE 22
SPERMATOGENIC FAILURE 22 		0.700 GeneticVariation UNIPROT A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. 28206990

2017