| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2493141 | 1 | 230729374 | intron variant | G/A;T | snv | 3 | |||||
| rs2760061 | 1 | 228003374 | upstream gene variant | T/A | snv | 0.55 | 3 | ||||
| rs2761436 | 1 | 207746403 | intergenic variant | C/A;T | snv | 3 | |||||
| rs2990220 | 1 | 155220463 | intron variant | T/A;C;G | snv | 3 | |||||
| rs35479618 | 1 | 153689947 | missense variant | G/A | snv | 9.5E-03 | 1.1E-02 | 3 | |||
| rs3753581 | 1 | 11860132 | upstream gene variant | C/A;T | snv | 3 | |||||
| rs4335411 | 1.000 | 1 | 248897507 | regulatory region variant | G/A | snv | 0.82 | 3 | |||
| rs6669371 | 1 | 11822085 | intron variant | T/G | snv | 0.14 | 3 | ||||
| rs11102916 | 1 | 115294125 | intron variant | C/A | snv | 3.7E-02 | 2 | ||||
| rs12405515 | 1 | 172388301 | intron variant | G/A;C;T | snv | 2 | |||||
| rs12741980 | 1 | 11879536 | non coding transcript exon variant | A/C | snv | 5.8E-02 | 2 | ||||
| rs1620668 | 1 | 112481358 | intron variant | A/G | snv | 0.17 | 2 | ||||
| rs182770070 | 1 | 9940418 | intron variant | A/T | snv | 5.8E-03 | 2 | ||||
| rs202071545 | 1 | 11818105 | intron variant | AAAA/-;AAA;AAAAA;AAAAAA | delins | 2 | |||||
| rs202102042 | 1.000 | 1 | 11847114 | missense variant | C/T | snv | 2.2E-04 | 1.6E-04 | 2 | ||
| rs2076460 | 1 | 27645547 | upstream gene variant | G/C;T | snv | 2 | |||||
| rs2404715 | 1.000 | 0.040 | 1 | 56543106 | intron variant | C/T | snv | 7.6E-02 | 2 | ||
| rs2493292 | 1 | 3412095 | missense variant | C/T | snv | 0.12; 4.4E-06 | 0.14 | 2 | |||
| rs2493296 | 1 | 3410468 | intron variant | C/G;T | snv | 2 | |||||
| rs351364 | 1 | 112502439 | intron variant | A/C;T | snv | 0.72 | 2 | ||||
| rs35295665 | 1 | 10737371 | intron variant | -/C | delins | 2 | |||||
| rs4320727 | 1.000 | 0.040 | 1 | 25025090 | downstream gene variant | G/A;C | snv | 2 | |||
| rs4653889 | 1 | 227924420 | intron variant | A/G | snv | 0.51 | 0.56 | 2 | |||
| rs4926923 | 1 | 47643553 | regulatory region variant | T/C | snv | 0.11 | 2 | ||||
| rs55892892 | 1 | 11836799 | intron variant | C/A | snv | 4.6E-02 | 2 |