FOXG1, forkhead box G1, 2290

N. diseases: 224; N. variants: 51
Disease: Congenital microcephaly ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555321402
rs1555321402
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
CUI: C2677180
Disease:
Congenital microcephaly 		C 0.700 GeneticVariation CLINVAR