Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606995
rs267606995
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B
CUI: C1846038
Disease:
MENTAL RETARDATION, X-LINKED 72
T 0.700 CausalMutation CLINVAR