Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk
Nature genetics, 2014•nature.com
Blood lipid levels are heritable, treatable risk factors for cardiovascular disease. We
systematically assessed genome-wide coding variation to identify new genes influencing
lipid traits, fine map known lipid loci and evaluate whether low-frequency variants with large
effects exist for these traits. Using an exome array, we genotyped 80,137 coding variants in
5,643 Norwegians. We followed up 18 variants in 4,666 Norwegians and identified ten loci
with coding variants associated with a lipid trait (P< 5× 10− 8). One variant in TM6SF2 …
systematically assessed genome-wide coding variation to identify new genes influencing
lipid traits, fine map known lipid loci and evaluate whether low-frequency variants with large
effects exist for these traits. Using an exome array, we genotyped 80,137 coding variants in
5,643 Norwegians. We followed up 18 variants in 4,666 Norwegians and identified ten loci
with coding variants associated with a lipid trait (P< 5× 10− 8). One variant in TM6SF2 …
Abstract
Blood lipid levels are heritable, treatable risk factors for cardiovascular disease. We systematically assessed genome-wide coding variation to identify new genes influencing lipid traits, fine map known lipid loci and evaluate whether low-frequency variants with large effects exist for these traits. Using an exome array, we genotyped 80,137 coding variants in 5,643 Norwegians. We followed up 18 variants in 4,666 Norwegians and identified ten loci with coding variants associated with a lipid trait (P < 5 × 10−8). One variant in TM6SF2 (encoding p.Glu167Lys), residing in a known genome-wide association study locus for lipid traits, influences total cholesterol levels and is associated with myocardial infarction. Transient TM6SF2 overexpression or knockdown of Tm6sf2 in mice alters serum lipid profiles, consistent with the association observed in humans, identifying TM6SF2 as a functional gene within a locus previously known as NCAN-CILP2-PBX4 or 19p13. This study demonstrates that systematic assessment of coding variation can quickly point to a candidate causal gene.
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