A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Much of the variation in inherited risk of colorectal cancer (CRC) is probably due to combinations of common low risk variants. We conducted a genome-wide association study of 550,000 tag SNPs in 930 familial colorectal tumor cases and 960 controls. The most strongly associated SNP (P = 1.72 x 10(-7...
Principais autores: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Journal article |
Idioma: | English |
Publicado em: |
2007
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