| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs846906 | 1.000 | 0.040 | 1 | 209714373 | intron variant | T/A;C | snv | 1 | |||
| rs11187033 | 1.000 | 0.040 | 10 | 92502602 | intron variant | T/A | snv | 0.28 | 1 | ||
| rs1479355 | 1.000 | 0.040 | 6 | 160109594 | 3 prime UTR variant | T/C | snv | 0.31 | 1 | ||
| rs369953112 | 1.000 | 0.040 | 7 | 22731416 | missense variant | T/C | snv | 1 | |||
| rs1559509 | 1.000 | 0.040 | 2 | 118098351 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs11123469 | 1.000 | 0.040 | 2 | 118086607 | upstream gene variant | T/C | snv | 0.14 | 1 | ||
| rs3780378 | 1.000 | 0.040 | 9 | 5112288 | non coding transcript exon variant | C/T | snv | 0.51 | 1 | ||
| rs138295501 | 1.000 | 0.040 | 11 | 128911903 | missense variant | G/A | snv | 2.2E-04 | 1.6E-04 | 1 | |
| rs760034984 | 1.000 | 0.040 | 19 | 11120434 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs3790433 | 1.000 | 0.040 | 1 | 65428659 | intron variant | C/G;T | snv | 1 | |||
| rs17482310 | 1.000 | 0.040 | 8 | 19889365 | regulatory region variant | G/C;T | snv | 1 | |||
| rs10185316 | 1.000 | 0.040 | 2 | 118086902 | upstream gene variant | C/G | snv | 0.32 | 1 | ||
| rs10085637 | 1.000 | 0.040 | 7 | 95596501 | 5 prime UTR variant | T/C;G | snv | 0.40 | 1 | ||
| rs295 | 1.000 | 0.040 | 8 | 19958727 | intron variant | A/C | snv | 0.28 | 1 | ||
| rs915654 | 1.000 | 0.040 | 6 | 31570720 | upstream gene variant | T/A;C | snv | 0.40 | 1 | ||
| rs7045890 | 1.000 | 0.040 | 9 | 94177906 | non coding transcript exon variant | G/A | snv | 0.93 | 1 | ||
| rs2294901 | 1.000 | 0.040 | 20 | 10404855 | 3 prime UTR variant | A/G | snv | 0.14 | 1 | ||
| rs6077785 | 1.000 | 0.040 | 20 | 10430806 | intron variant | A/C;T | snv | 1 | |||
| rs6108572 | 1.000 | 0.040 | 20 | 10432111 | intron variant | A/T | snv | 0.52 | 1 | ||
| rs6133922 | 1.000 | 0.040 | 20 | 10420425 | intron variant | A/G | snv | 6.4E-02 | 1 | ||
| rs2963156 | 1.000 | 0.040 | 5 | 143378931 | intron variant | T/A;C | snv | 1 | |||
| rs2233546 | 1.000 | 0.040 | 11 | 77102915 | missense variant | C/A;G;T | snv | 1.4E-04; 4.1E-06; 7.0E-02 | 1 | ||
| rs2233549 | 1.000 | 0.040 | 11 | 77103064 | synonymous variant | G/A | snv | 0.22 | 0.21 | 1 | |
| rs1055419 | 1.000 | 0.040 | 3 | 125594988 | 5 prime UTR variant | G/A | snv | 7.6E-02 | 1 | ||
| rs2179706 | 1.000 | 0.040 | 20 | 57564815 | non coding transcript exon variant | C/T | snv | 0.44 | 1 |