Sensitive

Colorectal cancer

BMP4 · rs4444235

Share:

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Colorectal cancer compared to the general population. (GWAS Catalog, Nat Genet 2008, PMID:19011631)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Colorectal cancer. (GWAS Catalog, Nat Genet 2008, PMID:19011631)
T/T Published research associates this genotype with typical/baseline likelihood of Colorectal cancer — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2008, PMID:19011631)

Source: GWAS Catalog, Nat Genet 2008, PMID:19011631

Share:

← See all variants