rs11228565 - SMIM38 - MYEOV

Magnitude 2.8 · 1 study on file

Reported associations

  • Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility - Unknown journal (n.d.) · Unknown authors · PubMed 19767754

    ABSTRACT: We report a genome-wide association follow up study on prostate cancer. We identify four variants associated with the disease in European populations: rs10934853-A (OR = 1.12, P = 2.9×10−10) on 3q21.3, two moderately correlated (r2 = 0.07) variants on 8q24.21; rs16902094-G (OR = 1.21, P = 6.2×10−15) and rs445114-T (OR = 1.14, P = 4.7×10−10) and rs8102476-C (OR = 1.12, P = 1.6×10−11) on 19q13.2. We also refine a previous association signal on 11q13 with the SNP rs11228565-A (OR =1.23, P = 6.7 × 10−12). In a multi-variant analysis, using 22 prostate cancer risk variants typed in the Icelandic population, we estimate that carriers belonging to the top 1.3% of the risk distribution have a risk of developing the disease that is more than 2.5 times greater than the popul


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Screening

  • Prostate cancer screening consultation High

    rs11228565-A increases prostate cancer risk by approximately 23 percent per allele compared to reference allele

    Discuss individualized prostate cancer screening options and timing with physician