Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776056911
rs776056911
Entrez Id: 9126
Gene Symbol: SMC3
SMC3
CUI: C1853099
Disease:
Cornelia de Lange Syndrome 3
G 0.700 GeneticVariation CLINVAR