Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060499752
rs1060499752
Entrez Id: 7265;114825
Gene Symbol: TTC1;PWWP2A
TTC1;PWWP2A
CUI: C4021085
Disease:
Abnormality of brain morphology
G 0.700 GeneticVariation CLINVAR