Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3024505
rs3024505
CUI: C0002871
Disease: Anemia
Anemia 		0.010 GeneticVariation BEFREE In contrast, CD patients carrying C allele of rs3024505 had significantly increased risk of anemia and stricturing/penetrating behavior. 27558476

2016