MEIOB, meiosis specific with OB-fold, 254528

N. diseases: 14; N. variants: 2
Disease: SPERMATOGENIC FAILURE 22 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555472691
rs1555472691
Entrez Id: 254528
Gene Symbol: MEIOB
MEIOB
CUI: C4540179
Disease:
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