FMN2, formin 2, 56776

N. diseases: 88; N. variants: 27
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727502861
rs727502861
Entrez Id: 56776
Gene Symbol: FMN2
FMN2
CUI: C4015444
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47 		C 0.700 CausalMutation CLINVAR