Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103263
rs119103263
Entrez Id: 9927
Gene Symbol: MFN2
MFN2
CUI: C4551563
Disease:
Microcephaly (physical finding)
T 0.700 CausalMutation CLINVAR