Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554121453
rs1554121453
Entrez Id: 8831;100847012
Gene Symbol: SYNGAP1;MIR5004
SYNGAP1;MIR5004
CUI: C2675473
Disease:
Mental Retardation, Autosomal Dominant 5
C 0.700 GeneticVariation CLINVAR