Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913678
rs121913678
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121913678
rs121913678
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 CausalMutation CLINVAR