| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4760 | 1.000 | 0.080 | 19 | 43648948 | missense variant | A/G | snv | 0.12 | 0.11 | 8 | |
| rs439680 | 1.000 | 0.080 | 5 | 109998341 | regulatory region variant | C/G | snv | 3 | |||
| rs121913297 | 1.000 | 0.080 | 13 | 48465028 | stop gained | G/A;T | snv | 2 | |||
| rs1360583020 | 1.000 | 0.080 | 12 | 120215202 | missense variant | G/C | snv | 4.3E-06 | 2 | ||
| rs942190 | 1.000 | 0.080 | 14 | 89956320 | intron variant | T/C | snv | 0.37 | 2 | ||
| rs10118776 | 1.000 | 0.080 | 9 | 6227418 | intron variant | G/A | snv | 0.94 | 1 | ||
| rs114033761 | 1.000 | 0.080 | 6 | 31093784 | regulatory region variant | T/C | snv | 1 | |||
| rs117729306 | 1.000 | 0.080 | 11 | 8465623 | non coding transcript exon variant | T/C | snv | 7.3E-03 | 1 | ||
| rs121913295 | 1.000 | 0.080 | 13 | 48463741 | missense variant | G/T | snv | 1 | |||
| rs12200782 | 1.000 | 0.080 | 6 | 26402808 | intron variant | C/G | snv | 7.9E-02 | 1 | ||
| rs12666409 | 1.000 | 0.080 | 7 | 50567279 | upstream gene variant | T/A | snv | 0.21 | 1 | ||
| rs12981718 | 1.000 | 0.080 | 19 | 54064604 | upstream gene variant | G/A;T | snv | 1 | |||
| rs140013431 | 1.000 | 0.080 | 6 | 7770278 | intron variant | T/C | snv | 1.2E-02 | 1 | ||
| rs141670911 | 1.000 | 0.080 | 6 | 26581030 | intergenic variant | A/T | snv | 7.3E-02 | 1 | ||
| rs141877527 | 1.000 | 0.080 | 10 | 33497992 | intergenic variant | A/G | snv | 7.3E-03 | 1 | ||
| rs1429133479 | 1.000 | 0.080 | 22 | 25847461 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs17185553 | 1.000 | 0.080 | 9 | 17934122 | intron variant | G/C | snv | 6.5E-02 | 1 | ||
| rs1778335 | 1.000 | 0.080 | 10 | 22643219 | intron variant | T/C | snv | 0.27 | 1 | ||
| rs312599 | 1.000 | 0.080 | 5 | 143998425 | intergenic variant | C/T | snv | 0.33 | 1 | ||
| rs3134425 | 1.000 | 0.080 | 11 | 122838470 | intron variant | T/C | snv | 0.67 | 1 | ||
| rs587781495 | 1.000 | 0.080 | 17 | 7676005 | missense variant | C/T | snv | 1 | |||
| rs716274 | 1.000 | 0.080 | 11 | 103547430 | intergenic variant | A/G | snv | 0.51 | 1 | ||
| rs74501188 | 1.000 | 0.080 | 5 | 90931162 | 5 prime UTR variant | G/A | snv | 0.17 | 1 | ||
| rs750078923 | 1.000 | 0.080 | 22 | 25769052 | missense variant | G/A;C | snv | 1.6E-05 | 1 | ||
| rs7519667 | 1.000 | 0.080 | 1 | 241722005 | intron variant | C/T | snv | 0.78 | 1 |