| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12752888 | 0.851 | 0.160 | 1 | 54527266 | downstream gene variant | T/C | snv | 0.26 | 4 | ||
| rs80356734 | 0.851 | 0.160 | 1 | 11022464 | missense variant | A/G | snv | 4 | |||
| rs80356773 | 0.925 | 0.080 | 1 | 155235002 | missense variant | C/T | snv | 3 | |||
| rs1315695444 | 1.000 | 0.040 | 1 | 169611580 | missense variant | C/G | snv | 4.0E-06 | 1.4E-05 | 2 | |
| rs564919438 | 1.000 | 0.040 | 1 | 45332421 | missense variant | G/C;T | snv | 8.0E-06 | 2 | ||
| rs115199861 | 1.000 | 0.040 | 1 | 171670879 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs115700680 | 1.000 | 0.040 | 1 | 171381070 | intergenic variant | T/G | snv | 1.9E-02 | 1 | ||
| rs115764752 | 1.000 | 0.040 | 1 | 171778066 | upstream gene variant | T/C | snv | 7.9E-03 | 1 | ||
| rs116065238 | 1.000 | 0.040 | 1 | 171482283 | upstream gene variant | A/G | snv | 4.3E-03 | 1 | ||
| rs55961051 | 1.000 | 0.040 | 1 | 20772323 | intron variant | G/A | snv | 5.5E-03 | 1 | ||
| rs61819372 | 1.000 | 0.040 | 1 | 113529488 | intron variant | C/A | snv | 6.8E-03 | 1 | ||
| rs74434895 | 1.000 | 0.040 | 1 | 113391450 | intron variant | G/A | snv | 6.8E-03 | 1 | ||
| rs74852193 | 1.000 | 0.040 | 1 | 68698339 | non coding transcript exon variant | G/A | snv | 3.8E-02 | 1 | ||
| rs7512924 | 1.000 | 0.040 | 1 | 246021301 | intron variant | T/C | snv | 0.25 | 1 | ||
| rs75578006 | 1.000 | 0.040 | 1 | 21019611 | intron variant | G/A | snv | 6.2E-03 | 1 | ||
| rs78649275 | 1.000 | 0.040 | 1 | 21150540 | intron variant | T/C | snv | 5.5E-03 | 1 | ||
| rs6721961 | 0.672 | 0.520 | 2 | 177265309 | intron variant | T/C;G | snv | 0.89 | 24 | ||
| rs387906686 | 0.742 | 0.320 | 2 | 165310413 | missense variant | C/A;T | snv | 23 | |||
| rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
| rs587777630 | 0.716 | 0.440 | 2 | 190986921 | missense variant | G/A | snv | 16 | |||
| rs781587642 | 0.851 | 0.120 | 2 | 219250557 | missense variant | G/A;C | snv | 2.0E-05 | 6 | ||
| rs17746510 | 0.882 | 0.080 | 2 | 173019562 | intron variant | T/C;G | snv | 5 | |||
| rs544706237 | 0.851 | 0.120 | 2 | 79121649 | missense variant | A/G;T | snv | 8.0E-06; 5.2E-05 | 5 | ||
| rs11887120 | 0.882 | 0.080 | 2 | 25262866 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs1427575965 | 0.925 | 0.120 | 2 | 70212796 | missense variant | G/A | snv | 8.0E-06 | 3 |