SNP associated_with study cohort

Subject: SNP
Relation: associated_with
Object: study cohort
p-value: 0.05

Evidence from: primary | all sources

Evidence (6 sources)

A saturated map of common genetic variants associated with human height. (2022) PMID:36224396 cited

correlation of SNP effects ... between discovery and replication ... expected correlation between estimated SNP effects in the discovery and replication sample

confidence: 0.90

A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism. (2015) PMID:26407342 cited

We ran association analyses separately in each of the three cohorts conditioning on our SNP with the lowest p-value...

confidence: 0.95

Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012) PMID:22605921 cited

This multi-pronged approach gave a total of 86 SNPs to test in the replication cohort.

confidence: 0.95

Genome-wide association study of bipolar disorder in European American and African American individuals. (2009) PMID:19488044 cited

performed replication genotyping of our most strongly associated SNPs on an independent cohort

confidence: 0.95

Genetic structure of Europeans: a view from the North-East. (2009) PMID:19424496 cited

The significance of the mean r2 values between cohorts was tested with the one-tailed t-test and p-value≤0.05 was considered as statistically significant.

confidence: 0.90

Marker selection for genetic case-control association studies. (2009) PMID:19390530 cited

important in a replication study, where the ability to replicate hinges on the genotyping accuracy of the SNP

confidence: 0.90