| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10046 | 0.708 | 0.400 | 15 | 51210789 | 3 prime UTR variant | G/A | snv | 0.45 | 0.43 | 18 | |
| rs10129516 | 1.000 | 0.040 | 14 | 63133372 | intron variant | T/A;C | snv | 1 | |||
| rs10131751 | 1.000 | 0.040 | 14 | 28212010 | intergenic variant | C/A | snv | 9.2E-02 | 1 | ||
| rs10167914 | 1.000 | 0.040 | 2 | 112805784 | TF binding site variant | A/G | snv | 0.31 | 1 | ||
| rs10282436 | 1.000 | 0.040 | 7 | 25833490 | upstream gene variant | G/T | snv | 0.19 | 1 | ||
| rs1037189404 | 0.776 | 0.280 | 1 | 155187519 | missense variant | C/T | snv | 8 | |||
| rs10419023 | 1.000 | 0.040 | 19 | 48427965 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
| rs10508881 | 1.000 | 0.040 | 10 | 44046117 | regulatory region variant | A/G | snv | 0.50 | 1 | ||
| rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
| rs1055144 | 1.000 | 0.040 | 7 | 25831489 | non coding transcript exon variant | C/T | snv | 0.16 | 3 | ||
| rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
| rs1065780 | 1.000 | 0.040 | 7 | 45888078 | upstream gene variant | G/A | snv | 0.39 | 1 | ||
| rs10757272 | 0.851 | 0.160 | 9 | 22088261 | intron variant | C/T | snv | 0.41 | 6 | ||
| rs10777670 | 1.000 | 0.040 | 12 | 95181055 | intron variant | G/A | snv | 0.23 | 1 | ||
| rs10794288 | 1.000 | 0.040 | 11 | 1086825 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs10835638 | 0.925 | 0.080 | 11 | 30230805 | intron variant | G/A;T | snv | 2 | |||
| rs10859856 | 1.000 | 0.040 | 12 | 95237500 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs10859871 | 1.000 | 0.040 | 12 | 95318100 | intron variant | A/C | snv | 0.37 | 2 | ||
| rs10895068 | 0.752 | 0.240 | 11 | 101129483 | 5 prime UTR variant | C/T | snv | 3.6E-02 | 14 | ||
| rs10902088 | 1.000 | 0.040 | 11 | 1090036 | non coding transcript exon variant | T/C | snv | 0.73 | 2 | ||
| rs10917151 | 0.925 | 0.040 | 1 | 22096228 | 3 prime UTR variant | G/A | snv | 0.14 | 3 | ||
| rs10953316 | 1.000 | 0.040 | 7 | 101038481 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.64 | 1 | ||
| rs10965235 | 1.000 | 0.040 | 9 | 22115106 | intron variant | C/A | snv | 0.15 | 1 |