Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776884
rs587776884
Entrez Id: 5932
Gene Symbol: RBBP8
RBBP8
CUI: C0796063
Disease:
microcephaly-digital anomalies syndrome
C 0.700 CausalMutation CLINVAR