| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2238032 | 0.925 | 0.040 | 12 | 2113566 | intron variant | T/C;G | snv | 2 | |||
| rs2283368 | 1.000 | 0.040 | 13 | 33019132 | intron variant | T/C | snv | 0.15 | 2 | ||
| rs2303579 | 0.925 | 0.040 | 15 | 55860531 | missense variant | T/C | snv | 0.74 | 0.72 | 2 | |
| rs3088077 | 0.925 | 0.040 | 15 | 55827379 | 3 prime UTR variant | C/T | snv | 0.20 | 2 | ||
| rs457274 | 1.000 | 0.040 | 21 | 41420558 | 5 prime UTR variant | C/G | snv | 0.35 | 2 | ||
| rs469083 | 1.000 | 0.040 | 21 | 41436789 | intron variant | C/T | snv | 0.61 | 2 | ||
| rs564919438 | 1.000 | 0.040 | 1 | 45332421 | missense variant | G/C;T | snv | 8.0E-06 | 2 | ||
| rs772720363 | 1.000 | 0.040 | 20 | 63350819 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs7759295 | 1.000 | 0.040 | 6 | 41168112 | upstream gene variant | C/G;T | snv | 2 | |||
| rs9526984 | 1.000 | 0.040 | 13 | 33035800 | intron variant | A/G | snv | 5.5E-02 | 2 | ||
| rs1039049 | 1.000 | 0.040 | 4 | 80416472 | intron variant | G/A | snv | 0.98 | 1 | ||
| rs1041536 | 1.000 | 0.040 | 20 | 9907627 | intergenic variant | T/C | snv | 0.46 | 1 | ||
| rs111231532 | 1.000 | 0.040 | 3 | 39135911 | intron variant | C/T | snv | 5.0E-02 | 1 | ||
| rs111600634 | 1.000 | 0.040 | 9 | 117856347 | intron variant | T/G | snv | 1.5E-02 | 1 | ||
| rs112961612 | 1.000 | 0.040 | 20 | 41872026 | intergenic variant | T/A | snv | 8.2E-02 | 1 | ||
| rs113793030 | 1.000 | 0.040 | 10 | 70287104 | upstream gene variant | T/C | snv | 1.7E-02 | 1 | ||
| 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 | ||
| rs116237496 | 1.000 | 0.040 | 8 | 101033687 | upstream gene variant | T/C | snv | 4.0E-02 | 1 | ||
| rs117070989 | 1.000 | 0.040 | 6 | 137490510 | downstream gene variant | C/A | snv | 8.3E-03 | 1 | ||
| rs117129097 | 1.000 | 0.040 | 12 | 128054737 | intron variant | C/G;T | snv | 1.9E-03 | 1 | ||
| rs117224174 | 1.000 | 0.040 | 6 | 114654261 | intergenic variant | G/A | snv | 2.2E-02 | 1 | ||
| rs117529438 | 1.000 | 0.040 | 12 | 64979216 | intron variant | C/T | snv | 3.4E-02 | 1 |