FMN2, formin 2, 56776

N. diseases: 88; N. variants: 27
Disease: Global developmental delay ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757511770
rs757511770
Entrez Id: 56776
Gene Symbol: FMN2
FMN2
CUI: C0557874
Disease:
Global developmental delay 		T 0.700 GeneticVariation CLINVAR