Sensitive
Colorectal cancer
BMP4 · rs4444235
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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
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