| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10845640 | 1.000 | 0.040 | 12 | 7659861 | intron variant | C/T | snv | 0.34 | 1 | ||
| rs5750146 | 1.000 | 0.040 | 22 | 35660681 | 3 prime UTR variant | G/A | snv | 8.7E-02 | 1 | ||
| rs5999924 | 1.000 | 0.040 | 22 | 35660097 | 3 prime UTR variant | A/G;T | snv | 1 | |||
| rs7118999 | 1.000 | 0.040 | 11 | 116774559 | 3 prime UTR variant | C/A;T | snv | 1 | |||
| rs1127065 | 1.000 | 0.040 | 7 | 44220272 | synonymous variant | C/G;T | snv | 1.7E-02; 0.41 | 1 | ||
| rs2953171 | 1.000 | 0.040 | 2 | 240596636 | non coding transcript exon variant | C/T | snv | 0.19 | 0.16 | 1 | |
| rs4945140 | 1.000 | 0.040 | 11 | 77074406 | intron variant | G/A;C | snv | 1 | |||
| rs13246513 | 1.000 | 0.040 | 7 | 80677435 | 3 prime UTR variant | C/G;T | snv | 0.36 | 1 | ||
| rs778035915 | 1.000 | 0.040 | 12 | 101698057 | missense variant | A/G | snv | 3.4E-05 | 7.0E-06 | 1 | |
| rs1053239 | 1.000 | 0.040 | 3 | 9867065 | 3 prime UTR variant | G/C | snv | 0.19; 5.6E-05 | 0.14 | 1 | |
| rs2479 | 1.000 | 0.040 | 3 | 9866841 | 3 prime UTR variant | A/G | snv | 0.79 | 1 | ||
| rs16944558 | 1.000 | 0.040 | 18 | 442441 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs2269383 | 1.000 | 0.040 | 22 | 50574346 | missense variant | C/T | snv | 2.6E-02 | 3.6E-02 | 1 | |
| rs6902771 | 1.000 | 0.040 | 6 | 151836746 | intron variant | C/T | snv | 0.45 | 1 | ||
| rs7774230 | 1.000 | 0.040 | 6 | 151843104 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs17782312 | 1.000 | 0.040 | 8 | 71220245 | intron variant | C/A | snv | 1 | |||
| rs715180 | 1.000 | 0.040 | 5 | 56001471 | intron variant | C/A | snv | 0.93 | 1 | ||
| rs4846922 | 1.000 | 0.040 | 1 | 230171436 | intron variant | T/A;C;G | snv | 1 | |||
| rs11760281 | 1.000 | 0.040 | 7 | 80475233 | intron variant | A/G | snv | 0.55 | 1 | ||
| rs1184436054 | 1.000 | 0.040 | 12 | 6843683 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs8177409 | 1.000 | 0.040 | 5 | 151020289 | upstream gene variant | A/T | snv | 0.15 | 1 | ||
| rs11066194 | 1.000 | 0.040 | 12 | 112212323 | intron variant | A/G | snv | 4.8E-02 | 1 | ||
| rs762861 | 1.000 | 0.040 | 4 | 3440284 | upstream gene variant | G/C | snv | 0.30 | 1 | ||
| rs736824 | 1.000 | 0.040 | 20 | 44406020 | intron variant | T/C | snv | 0.50 | 0.45 | 1 | |
| rs6130608 | 1.000 | 0.040 | 20 | 44395368 | intron variant | T/C | snv | 0.33 | 1 |