Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401820
rs1135401820
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C0750927
Disease:
Apraxia, Developmental Verbal
C 0.700 GeneticVariation CLINVAR