Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569545382
rs1569545382
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
CUI: C0016667
Disease:
Fragile X Syndrome
A 0.700 CausalMutation CLINVAR