FANCM, FA complementation group M, 57697

N. diseases: 147; N. variants: 11
Disease: SPERMATOGENIC FAILURE 28 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs147021911
rs147021911
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C4748117
Disease:
SPERMATOGENIC FAILURE 28 		T 0.700 CausalMutation CLINVAR