| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs74315406 | 0.851 | 0.160 | 20 | 4699870 | missense variant | A/G | snv | 5 | |||
| rs74315412 | 0.851 | 0.120 | 20 | 4699843 | missense variant | G/A | snv | 6.0E-05 | 3.5E-05 | 5 | |
| rs74315414 | 0.882 | 0.200 | 20 | 4699533 | missense variant | C/A;T | snv | 4.0E-06 | 5 | ||
| rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
| rs2814707 | 0.882 | 0.120 | 9 | 27536399 | non coding transcript exon variant | C/G;T | snv | 4 | |||
| rs1178466848 | 0.925 | 0.120 | 20 | 4699785 | missense variant | G/A | snv | 2.8E-05 | 4 | ||
| rs193922906 | 0.882 | 0.160 | 20 | 4699380 | inframe insertion | TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC/-;TCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC | delins | 4 | |||
| rs398122370 | 0.925 | 0.160 | 20 | 4699851 | missense variant | G/C | snv | 4 | |||
| rs74315411 | 0.882 | 0.160 | 20 | 4699767 | missense variant | A/G | snv | 4 | |||
| rs761807915 | 0.925 | 0.120 | 20 | 4699824 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs80356711 | 1.000 | 20 | 4699698 | stop gained | C/T | snv | 4 | ||||
| rs2736990 | 0.882 | 0.080 | 4 | 89757390 | intron variant | G/A;T | snv | 4 | |||
| rs597668 | 0.925 | 0.080 | 19 | 45205630 | intron variant | T/A;C;G | snv | 3 | |||
| rs368821179 | 0.925 | 0.160 | 17 | 80182758 | missense variant | T/C | snv | 8.0E-06 | 2.1E-05 | 3 | |
| rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 3 | ||
| rs1473972013 | 0.925 | 0.160 | 1 | 47035911 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs947211 | 0.925 | 0.040 | 1 | 205783537 | non coding transcript exon variant | A/G | snv | 0.64 | 3 | ||
| rs670139 | 0.925 | 0.080 | 11 | 60204322 | intron variant | G/A;T | snv | 3 | |||
| rs398122414 | 0.925 | 0.120 | 20 | 4699898 | stop gained | C/A | snv | 3 | |||
| rs751882709 | 0.925 | 0.160 | 20 | 4699855 | missense variant | A/C | snv | 1.6E-05 | 2.8E-05 | 3 | |
| rs80356710 | 0.925 | 0.040 | 20 | 4699655 | stop gained | T/G | snv | 3 | |||
| rs10509125 | 10 | 60167108 | intron variant | C/A | snv | 0.56 | 2 | ||||
| rs10994443 | 1.000 | 0.040 | 10 | 60635760 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs4538475 | 1.000 | 0.040 | 4 | 15736314 | intron variant | A/G | snv | 0.24 | 2 | ||
| rs9349407 | 1.000 | 0.080 | 6 | 47485642 | intron variant | G/C | snv | 0.23 | 2 |