Rs16901979

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risk for prostate cancer
is asnp
is mentioned by
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23andMers16901979
SNP Nexus

Chromosome8
Orientationplus
Position128194097
GenotypeEffect
rs16901979(A;A)1.5x increased risk for prostate cancer
rs16901979(A;C)1.5x increased risk for prostate cancer
rs16901979(C;C)normal risk


Genotypes Magnitude Summary
Rs16901979(A;A) 2.92.9 1.5x increased risk for prostate cancer
Rs16901979(A;C) 2.92.9 1.5x increased risk for prostate cancer
Rs16901979(C;C) 00 normal risk
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This SNP has been recognized by the Coriell Personalized Medicine Collaborative ICOB.
Additional information is available here

rs16901979 is a SNP on chromosome 8q24, associated with increased risk for prostate cancer in several studies. In some studies, the regions have been divided, and this SNP falls in region 2.

In a study of over 3,600 Caucasians with prostate cancer, rs16901979 is one of five SNPs used (with family history as a sixth factor) to cumulatively predict overall risk. On their own, the rs16901979(A;A) and (A;C) risk genotypes yield an odds ratio for developing prostate cancer of 1.53 (CI: 1.22-1.92, p=1.8x10e-4) and may account for 3.6% of population attributable risk.10.1056/NEJMoa075819

cancer related according to this blog

Two genetic markers in the 8q24 region of chromosome 8 rs7008482 and rs16901979 have been linked to an increased risk of prostate cancer in African Americans. abstract

In follow-up studies looking at disease severity (and not just overall risk), this SNP is reported to account for the risk (from region 2) of advanced prostate cancer.[PMID 18231127]]

A meta-analysis of 10+ studies comprising over 15,000 prostate cancer patients concluded that the odds ratio for rs16901979(A) allele carriers is 1.74 (CI: 1.72-1.77).[PMID 18231127]

? (A;A) (A;C) (C;C)
GWAS
SNP rs16901979
PubMedID [PMID 17401366]
Condition Prostate cancer
Gene Intergenic
Risk Allele A
pValue 1.00E-012
OR 1.79
95% CI 1.53-2.11) (EA
Neighborrs10505483
Distance279


[PMID 19549807] Prostate Cancer Risk Associated Loci in African Americans

[PMID 19562729] Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry

Related to PROSTATE CANCER, HEREDITARY, 10; HPC10 according to omim 611100. See also
GWAS snp
PMID [PMID 19767754]
Trait Prostate cancer
Title Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Risk Allele A
P-val 3E-14
Odds Ratio 1.80 [1.55-2.09]

[PMID 19908238] Common variants at 8q24 are associated with prostate cancer risk in Taiwanese men

PharmGKBPA162356603
Name
AnnotationGWAS Results: Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 (Initial Sample Size: 1,435 cases, 3,064 controls; Replication Sample Size: 1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls; Risk Allele: rs16901979-A).
GeneSRRM1L
Featue
EvidencePubMed ID:17401366; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesProstatic Neoplasms
Curation LevelNon-Curated