| Baseline Phenotype (GS clinic visit) | 2006–2011 | 3,228,900 (21,526 × 150) |
| Baseline Phenotype (GS Pre-Clinic Questionnaire) | 2006–2011 | 9,439,200 (23,598 × 400) |
| Genotype (genome-wide, after QC and imputation) | 2013–2016 | 24,111,857 imputed genetic |
| variants (20,032 IDs) | ||
| NHS EHR phenotype (biochemistry tests) | 2014–2015 | 2,192,346 (11,125 IDs) |
| NHS EHR phenotype (hospital in-patient episodes) | 2012–2015 | 106,492 (18,687 IDs) |
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