| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 10 | |||
| rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 7 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
| rs16903574 | 0.882 | 0.120 | 5 | 14610200 | missense variant | C/A;G | snv | 4.0E-06; 5.6E-02 | 6 | ||
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
| rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 5 | ||
| rs1700159 | 1.000 | 0.040 | 12 | 51912002 | intron variant | C/A;G;T | snv | 4 | |||
| rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 | |||
| rs10791824 | 0.882 | 0.160 | 11 | 65791795 | intron variant | A/G;T | snv | 3 | |||
| rs1214598 | 0.925 | 0.120 | 1 | 167457187 | non coding transcript exon variant | G/A;C;T | snv | 3 | |||
| rs2390314 | 0.925 | 0.120 | 7 | 20416355 | downstream gene variant | A/C;T | snv | 3 | |||
| rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 3 | |||
| rs10910095 | 1.000 | 0.040 | 1 | 2579316 | upstream gene variant | G/A;C | snv | 2 | |||
| rs11539209 | 1.000 | 0.040 | 9 | 128721272 | missense variant | T/A;C | snv | 7.4E-02 | 2 | ||
| rs250308 | 1.000 | 0.040 | 5 | 119348602 | intron variant | T/A;C | snv | 2 | |||
| rs62117160 | 0.925 | 0.120 | 19 | 44728895 | upstream gene variant | G/A;T | snv | 2 | |||
| rs1025549 | 1.000 | 0.040 | 2 | 198016459 | intron variant | G/A;T | snv | 1 | |||
| rs1032841 | 1.000 | 0.040 | 2 | 8526108 | intron variant | A/G;T | snv | 1 | |||
| rs10937319 | 1.000 | 0.040 | 3 | 187711669 | intron variant | T/A;C | snv | 1 | |||
| rs11916411 | 1.000 | 0.040 | 3 | 23526489 | intron variant | A/C;T | snv | 1 | |||
| rs1260294 | 1.000 | 0.040 | 12 | 123075742 | 5 prime UTR variant | T/A;C | snv | 1 | |||
| rs17057868 | 1.000 | 0.040 | 5 | 160487658 | downstream gene variant | T/A;C | snv | 1 | |||
| rs17389644 | 0.925 | 0.120 | 4 | 122576542 | intergenic variant | G/A;T | snv | 1 | |||
| rs1998266 | 1.000 | 0.040 | 6 | 36390512 | intron variant | T/A;C | snv | 1 |