Skip to main content
. 2021 Oct 26;375:n2233. doi: 10.1136/bmj.n2233

Table 4.

Description of GWAS consortiums used for each phenotype. Table reproduced with permission from Wootton et al, 201839

Variable First author (year) Consortium Sample size Population* Sex*
Subjective wellbeing Okbay25 (2016) SSGAC 298 420 100% European Mixed†
Body mass index Locke26 (2015) GIANT 339 224 95% European 53% female
Waist to hip ratio Shungin27 (2015) GIANT 210 088 100% European 56% female
Waist circumference Shungin27 (2015) GIANT 232 101 100% European 55% female
Body fat percentage Lu28 (2016) Not available 100 716 89% European 48% female
HDL cholesterol Willer29 (2013) GLGC 92 860 100% European Mixed†
LDL cholesterol Willer29 (2013) GLGC 83 198 100% European Mixed†
Total cholesterol Willer29 (2013) GLGC 92 260 100% European Mixed†
Coronary artery disease Nikpay30 (2015) CARDIoGRAMplusC4D Cases=60 801; controls=123 504 77% European Mixed†
Myocardial infarction Nikpay30 (2015) CARDIoGRAMplusC4D Cases=43 676; controls=128 199 Mixed† Mixed†
Diastolic blood pressure Wain31 (2017) Not available 150 134 100% European 60% female
Systolic blood pressure Wain31 (2017) Not available 150 134 100% European 60% female

SSGAC=Social Science Genetics Association Consortium; GLGC=Global Lipids Genetics Consortium; GIANT=Genetic Investigation of Anthropometric Traits consortium; HDL=high density lipoprotein; LDL=low density lipoprotein; GWAS=genome wide association study.

*

If not reported, percentage sex and European ancestry were calculated from contributing cohort data in the supplementary materials. All GWAS had similar sex ratios and ancestries included. The largest difference was between the consortiums for coronary artery disease and subjective wellbeing, which used 77% and 100% individuals of European ancestry, respectively. If two populations differ, two sample mendelian randomisation can still be used to test for a causal effect, but the magnitude of the effect might not be as precise.32

Information on the sex ratios and ancestry proportions for the whole sample were not reported or not possible to calculate in the CARDIoGRAMplusC4D, GLGC, and SSGAC consortiums.