Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205866
rs786205866
Entrez Id: 1917
Gene Symbol: EEF1A2
EEF1A2
CUI: C4225343
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 38
T 0.800 CausalMutation CLINVAR
dbSNP: rs786205866
rs786205866
Entrez Id: 1917
Gene Symbol: EEF1A2
EEF1A2
CUI: C4225343
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 38
0.800 GeneticVariation UNIPROT