Variant: rs11601507

present in Gene: TRIM5 present in Chromosome: 11 Position on Chromosome: 5679844 Alleles of this Variant: C/A;T

rs11601507 in TRIM5 gene and Coronary Artery Disease PMID 29212778 2018 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

rs11601507 in TRIM5 gene and Low density lipoprotein cholesterol measurement PMID 29507422 2018 A large electronic-health-record-based genome-wide study of serum lipids.

rs11601507 in TRIM5 gene and Platelet mean volume determination (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.