Table 1.
22 EA-Associated Type 2 Diabetes Quantitative Traits Loci with Substantially Reduced 99% Credible Sets Based on Trans-ethnic Fine Mapping
| Locusa | Chr |
99% Credible Set: European Ancestry Only |
99% Credible Set: Trans-ethnic |
99% Credible Set Reduction |
|||
|---|---|---|---|---|---|---|---|
| # SNPsb | Rangec(bp) | # SNPsb | Rangec(bp) | % SNPsd | % Rangee | ||
| Fasting Glucose-Associated Loci | |||||||
| FOXA2 | 20 | 40 | 46,365 | 2 | 3,872 | 95.0 | 91.6 |
| GCK | 7 | 7 | 25,107 | 1 | 1 | 85.7 | 100.0 |
| KL | 13 | 696 | 496,262 | 147 | 492,550 | 78.9 | 0.7 |
| ADCY5 | 3 | 4 | 31,042 | 1 | 1 | 75.0 | 100.0 |
| GCKR | 2 | 2 | 11,663 | 1 | 1 | 50.0 | 100.0 |
| PROX1 | 1 | 11 | 18,286 | 6 | 13,550 | 45.5 | 25.9 |
| DPYSL5 | 2 | 87 | 294,065 | 50 | 269,667 | 42.5 | –8.3 |
| IGF2BP2 | 3 | 64 | 317,522 | 38 | 355,236 | 40.6 | –11.9 |
| CDKN2B-ANRIL | 9 | 7 | 5,914 | 5 | 4,515 | 28.6 | 23.7 |
| ADRA2A | 10 | 33 | 68,716 | 26 | 68,110 | 21.2 | 0.9 |
| TCF7L2 | 10 | 5 | 36,312 | 4 | 15,268 | 20.0 | 58.0 |
| FADS1 | 11 | 20 | 58,394 | 16 | 57,823 | 20.0 | 1.0 |
| DGKB-TMEM195 | 7 | 11 | 143,605 | 10 | 2,182 | 9.1 | 98.5 |
| CRY2 | 11 | 10 | 57,088 | 11 | 14,850 | –10.0 | 74.0 |
| Fasting Insulin-Associated Loci | |||||||
| ARL15 | 5 | 319 | 498,585 | 22 | 33,535 | 93.1 | 93.3 |
| PPP1R3B | 8 | 8 | 9,510 | 1 | 1 | 87.5 | 100.0 |
| COBLL1-GRB14 | 2 | 14 | 51,528 | 3 | 11,540 | 78.6 | 77.6 |
| IRS1 | 2 | 43 | 137,640 | 13 | 68,951 | 69.8 | 49.9 |
| GCKR | 2 | 3 | 11,663 | 1 | 1 | 66.7 | 100.0 |
| FAM13A | 4 | 43 | 243,374 | 21 | 243,374 | 51.2 | 0.0 |
| ANKRD55-MAP3K1 | 5 | 417 | 497,027 | 218 | 487,103 | 47.7 | 2.0 |
| UHRF1BP1 | 6 | 13 | 217,136 | 9 | 136,609 | 30.8 | 37.1 |
| PPARG | 3 | 14 | 60,448 | 11 | 56,618 | 21.4 | 6.3 |
The 22 EA-associated T2D QT loci include 13 fasting glucose, 8 fasting insulin, and 1 associated with both. Substantial reduction is defined as greater than 20% reduction in its genomic length or the number of SNPs.
For ease of comparison to previous studies, the loci are named based on the historically identified nearest protein-coding gene or genes to the index SNP in European ancestry.
# SNPs is the number of SNPs included in the 99% credible set.
Range is defined as the maximum genomic distance based on hg18 among the SNPs included in the 99% credible set.
%SNPs is (the number of SNPs in the EA-based 99% credible set − the number of SNPs in the trans-ethnic analysis-based 99% credible set)/the number of SNPs in the EA-based 99% credible set.
%Range is (the range of the EA-based 99% credible set − the range of the trans-ethnic analysis-based 99% credible set)/the range of the EA-based 99% credible set.