rs11614062 - SOCS2-AS1

Magnitude 2.2 · 1 study on file

Reported associations

• Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants - Unknown journal (n.d.) · Unknown authors · PubMed 28270201

  ABSTRACT: Background The Generation Scotland: Scottish Family Health Study (GS:SFHS) is a family-based population cohort with DNA, biological samples, socio-demographic, psychological and clinical data from approximately 24,000 adult volunteers across Scotland. Although data collection was cross-sectional, GS:SFHS became a prospective cohort due to of the ability to link to routine Electronic Health Record (EHR) data. Over 20,000 participants were selected for genotyping using a large genome-wide array. Methods GS:SFHS was analysed using genome-wide association studies (GWAS) to test the effects of a large spectrum of variants, imputed using the Haplotype Research Consortium (HRC) dataset, on medically relevant traits measured directly or obtained from EHRs. The HRC dataset is the largest

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