FOXG1, forkhead box G1, 2290

N. diseases: 224; N. variants: 51
Disease: FOXG1 syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767961672
rs767961672
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
CUI: C3150705
Disease:
FOXG1 syndrome 		T 0.700 GeneticVariation CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784 2016