| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2668196 | 3 | 165784921 | intron variant | A/T | snv | 0.75 | 3 | ||||
| rs7581162 | 2 | 60477349 | intron variant | T/A | snv | 0.49 | 3 | ||||
| rs962369 | 11 | 27712873 | intron variant | T/C | snv | 0.24 | 3 | ||||
| rs8044363 | 0.925 | 0.040 | 16 | 1200559 | synonymous variant | T/A;C | snv | 0.37 | 3 | ||
| rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
| rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
| rs1149558 | 0.925 | 0.080 | 7 | 133363002 | intron variant | T/C;G | snv | 3 | |||
| rs9556958 | 1.000 | 0.040 | 13 | 98447792 | 3 prime UTR variant | C/G;T | snv | 3 | |||
| rs2764261 | 6 | 108606639 | intron variant | A/G;T | snv | 3 | |||||
| rs1167800 | 7 | 75546898 | intron variant | A/G | snv | 0.34 | 3 | ||||
| rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
| rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
| rs6731373 | 2 | 68275912 | intergenic variant | G/A | snv | 0.29 | 3 | ||||
| rs13262595 | 1.000 | 0.040 | 8 | 142235609 | intron variant | A/C;G | snv | 3 | |||
| rs6119267 | 20 | 32576112 | intron variant | C/A;G | snv | 3 | |||||
| rs76076331 | 1.000 | 0.040 | 2 | 10837459 | intron variant | C/T | snv | 1.0E-01 | 3 | ||
| rs11545169 | 3 | 184302754 | missense variant | G/T | snv | 0.13 | 0.11 | 3 | |||
| rs11765189 | 1.000 | 0.040 | 7 | 157743285 | intron variant | A/G | snv | 0.25 | 3 | ||
| rs75757892 | 6 | 7232156 | intron variant | C/T | snv | 0.12 | 3 | ||||
| rs9616914 | 1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 | 3 | |
| rs7218708 | 17 | 20023523 | intron variant | A/C;G | snv | 3 | |||||
| rs7963801 | 12 | 79291446 | intron variant | T/C | snv | 0.70 | 3 | ||||
| rs62154720 | 1.000 | 0.040 | 2 | 105306623 | intron variant | C/T | snv | 9.2E-02 | 3 | ||
| rs6870983 | 5 | 88401716 | intron variant | C/T | snv | 0.29 | 3 | ||||
| rs4396807 | 22 | 37742372 | intron variant | G/C | snv | 0.38 | 3 |