Variant: rs56848936 

    present in Gene: SYMPK
    present in Chromosome: 19
    Position on Chromosome: 45818249
    Alleles of this Variant: A/G

rs56848936 in SYMPK gene and Adenocarcinoma of large intestine PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and Colonic Neoplasms PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and Colorectal Carcinoma PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and Colorectal Neoplasms PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and Malignant neoplasm of large intestine PMID 28295283 2017 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

rs56848936 in SYMPK gene and Malignant tumor of colon PMID 28295283 2017 We identified a novel variant, rs56848936 in the gene SYMPK at 19q13.3, associated with colon cancer risk (odds ratio 0.61 for the risk allele G, p = 2.4 × 10<sup>-8</sup> ).