Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122908
rs398122908
Entrez Id: 3054;8269
Gene Symbol: HCFC1;TMEM187
HCFC1;TMEM187
CUI: C0796208
Disease:
MENTAL RETARDATION, X-LINKED 3
G 0.700 CausalMutation CLINVAR