Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863224008
rs863224008
Entrez Id: 2271
Gene Symbol: FH
FH
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 GeneticVariation CLINVAR