| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11646213 | 0.827 | 0.320 | 16 | 82609046 | intergenic variant | A/T | snv | 0.47 | 6 | ||
| rs11651270 | 0.882 | 0.240 | 17 | 5521757 | missense variant | T/C | snv | 0.45 | 0.47 | 4 | |
| rs11771443 | 0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 | 8 | ||
| rs1177506410 | 0.776 | 0.240 | 1 | 230706148 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 12 | |
| rs117897666 | 0.882 | 0.160 | 15 | 73811619 | intergenic variant | C/T | snv | 3 | |||
| rs11886047 | 1.000 | 0.120 | 2 | 43623451 | upstream gene variant | T/A;C | snv | 0.20 | 1 | ||
| rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 29 | ||
| rs11915160 | 0.851 | 0.200 | 3 | 181713783 | 3 prime UTR variant | C/A | snv | 0.11 | 5 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs12449782 | 0.925 | 0.200 | 17 | 63498888 | intron variant | G/A | snv | 0.41 | 3 | ||
| rs1249910 | 1.000 | 0.120 | 3 | 112672327 | intergenic variant | A/G | snv | 0.58 | 1 | ||
| rs12523822 | 1.000 | 0.120 | 6 | 154633286 | intergenic variant | C/G;T | snv | 1 | |||
| rs1252906 | 1.000 | 0.120 | 14 | 59192073 | intron variant | A/C;G | snv | 1 | |||
| rs1253192 | 1.000 | 0.120 | 14 | 59376688 | intergenic variant | A/G | snv | 0.92 | 1 | ||
| rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
| rs12708815 | 1.000 | 0.120 | 16 | 17134511 | synonymous variant | G/A;C | snv | 0.56 | 1 | ||
| rs1275805226 | 0.776 | 0.240 | 1 | 230706148 | frameshift variant | G/- | del | 7.0E-06 | 12 | ||
| rs12976445 | 0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 | 20 | ||
| rs1298908 | 1.000 | 0.120 | 10 | 80253378 | non coding transcript exon variant | C/T | snv | 0.48 | 0.53 | 1 | |
| rs13254600 | 1.000 | 0.120 | 8 | 123077286 | intron variant | C/A;G | snv | 0.28; 4.8E-06 | 1 | ||
| rs1326934 | 0.925 | 0.200 | 10 | 95524324 | intron variant | C/T | snv | 0.63 | 2 | ||
| rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
| rs1341633213 | 1.000 | 0.120 | 17 | 63496422 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs1345365 | 1.000 | 0.120 | 7 | 37161008 | intron variant | G/A | snv | 0.61 | 1 | ||
| rs136161 | 0.925 | 0.160 | 22 | 36261386 | intron variant | G/C | snv | 0.51 | 3 |