Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518770
rs1057518770
Entrez Id: 7337;104472715
Gene Symbol: UBE3A;SNHG14
UBE3A;SNHG14
CUI: C1842581
Disease:
Abnormal corpus callosum morphology
T 0.700 CausalMutation CLINVAR