| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs748405415 | 0.790 | 0.160 | 7 | 142773993 | stop gained | G/A;T | snv | 8 | |||
| rs202003805 | 0.827 | 0.120 | 7 | 142750561 | missense variant | C/T | snv | 9.0E-05 | 6 | ||
| rs113857788 | 0.882 | 0.160 | 7 | 117664780 | missense variant | G/C;T | snv | 1.0E-03; 6.0E-05 | 5 | ||
| rs139729994 | 0.925 | 0.120 | 7 | 117614713 | missense variant | G/A;T | snv | 4.0E-06; 1.3E-04 | 2 | ||
| rs1554499091 | 0.925 | 0.040 | 7 | 142751884 | missense variant | T/C | snv | 2 | |||
| rs752688735 | 0.925 | 0.040 | 7 | 142752547 | missense variant | G/A | snv | 2 | |||
| rs371282890 | 0.827 | 0.120 | 8 | 19955900 | missense variant | C/G | snv | 1.1E-04 | 6.3E-05 | 6 | |
| rs773891125 | 0.827 | 0.120 | 8 | 19955896 | frameshift variant | CT/- | delins | 6 | |||
| rs118204082 | 0.851 | 0.120 | 8 | 19955863 | missense variant | C/G;T | snv | 1.5E-04 | 4 | ||
| rs587777636 | 0.882 | 0.080 | 8 | 143213935 | missense variant | G/A;C | snv | 6.5E-06 | 4 | ||
| rs747940576 | 0.882 | 0.120 | 8 | 11853351 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 4 | |
| rs761886494 | 0.925 | 0.040 | 8 | 19955870 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 3 | |
| rs11988997 | 1.000 | 0.040 | 8 | 118753955 | intron variant | C/T | snv | 7.4E-02 | 1 | ||
| rs762727745 | 1.000 | 0.040 | 8 | 11847803 | synonymous variant | G/A | snv | 1.7E-05 | 1 | ||
| rs142022985 | 1.000 | 0.040 | 9 | 33798530 | missense variant | A/G | snv | 1.2E-03 | 1.5E-03 | 1 | |
| rs2995271 | 0.925 | 0.040 | 10 | 30230903 | regulatory region variant | C/T | snv | 0.64 | 2 | ||
| rs4751995 | 1.000 | 0.040 | 10 | 116638373 | splice acceptor variant | A/G;T | snv | 0.49 | 0.55 | 1 | |
| rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
| rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 15 | |||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs11554495 | 0.701 | 0.240 | 12 | 52904798 | missense variant | C/A | snv | 4.9E-03 | 5.4E-03 | 19 | |
| rs1303 | 0.925 | 0.040 | 14 | 94378506 | missense variant | T/G | snv | 0.28 | 0.22 | 4 | |
| rs777418530 | 0.763 | 0.120 | 16 | 84845883 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 10 | |
| rs1413293653 | 1.000 | 0.040 | 16 | 84866923 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs775626498 | 1.000 | 0.040 | 16 | 84850577 | missense variant | G/A | snv | 1 |