| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs743572 | 0.672 | 0.360 | 10 | 102837395 | 5 prime UTR variant | A/G;T | snv | 0.40; 8.1E-06 | 24 | ||
| rs1805097 | 0.689 | 0.360 | 13 | 109782884 | missense variant | C/G;T | snv | 0.35 | 22 | ||
| rs1445081098 | 0.724 | 0.480 | 22 | 19963746 | missense variant | G/C | snv | 4.0E-06 | 17 | ||
| rs1131445 | 0.724 | 0.440 | 15 | 81309441 | 3 prime UTR variant | T/A;C | snv | 16 | |||
| rs605059 | 0.763 | 0.160 | 17 | 42554888 | missense variant | G/A;C;T | snv | 0.56; 9.0E-05; 1.4E-05 | 15 | ||
| rs2854746 | 0.752 | 0.200 | 7 | 45921046 | missense variant | G/A;C;T | snv | 0.38 | 14 | ||
| rs6165 | 0.724 | 0.160 | 2 | 48963902 | missense variant | C/G;T | snv | 4.0E-06; 0.55 | 14 | ||
| rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
| rs1550117 | 0.790 | 0.320 | 2 | 25343038 | upstream gene variant | A/G;T | snv | 11 | |||
| rs1181860747 | 0.776 | 0.240 | 19 | 7122961 | missense variant | C/T | snv | 10 | |||
| rs2237895 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 10 | |||
| rs3756712 | 0.790 | 0.160 | 5 | 308981 | non coding transcript exon variant | A/C;T | snv | 10 | |||
| rs763000109 | 0.827 | 0.240 | 6 | 31575788 | missense variant | C/G;T | snv | 4.1E-06; 1.6E-05 | 9 | ||
| rs1037189404 | 0.776 | 0.280 | 1 | 155187519 | missense variant | C/T | snv | 8 | |||
| rs2294021 | 0.776 | 0.280 | X | 49249149 | intron variant | T/A;C | snv | 0.52 | 8 | ||
| rs2812378 | 0.790 | 0.200 | 9 | 34710263 | intron variant | G/A;C | snv | 8 | |||
| rs113593938 | 0.790 | 0.200 | 21 | 44250907 | missense variant | C/T | snv | 3.5E-03 | 7 | ||
| rs2066479 | 0.790 | 0.160 | 9 | 96235528 | missense variant | C/A;G;T | snv | 7.2E-02 | 7 | ||
| rs2292596 | 0.827 | 0.240 | 5 | 422840 | missense variant | C/G;T | snv | 0.38; 4.0E-06 | 7 | ||
| rs7354779 | 0.827 | 0.200 | 21 | 44250887 | missense variant | T/C | snv | 0.21 | 6 | ||
| rs334348 | 0.851 | 0.160 | 9 | 99150189 | 3 prime UTR variant | A/G;T | snv | 5 | |||
| rs2246901 | 0.882 | 0.080 | 3 | 195762138 | missense variant | C/A;T | snv | 0.67 | 3 | ||
| rs2475335 | 0.882 | 0.080 | 9 | 10260263 | intron variant | C/A;T | snv | 3 | |||
| rs372201428 | 0.882 | 0.120 | 17 | 7676181 | missense variant | G/A;C | snv | 1.2E-05 | 3 | ||
| rs4980524 | 0.882 | 0.080 | 11 | 64191787 | intron variant | A/C;T | snv | 3 |