| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1525489 | 1.000 | 0.080 | 7 | 122993419 | downstream gene variant | A/G | snv | 3.6E-02 | 1 | ||
| rs17239025 | 1.000 | 0.080 | 13 | 30765768 | downstream gene variant | G/C | snv | 4.1E-02 | 1 | ||
| rs2228545 | 1.000 | 0.080 | 2 | 202555989 | missense variant | G/A | snv | 2.4E-02 | 2.2E-02 | 1 | |
| rs2705535 | 1.000 | 0.080 | 3 | 112490080 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs770507184 | 1.000 | 0.080 | 19 | 45370161 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs10857561 | 1.000 | 0.080 | 10 | 48400595 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs202195689 | 1.000 | 0.080 | 4 | 7460097 | mature miRNA variant | -/C;CACCC;CCC | delins | 1 | |||
| rs4796535 | 1.000 | 0.080 | 17 | 6656544 | intron variant | G/A | snv | 3.9E-03 | 1 | ||
| rs767285340 | 1.000 | 0.080 | 2 | 47799861 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||
| rs5743030 | 1.000 | 0.080 | 2 | 189813819 | intron variant | G/A | snv | 0.11 | 1 | ||
| rs5743100 | 1.000 | 0.080 | 2 | 189841127 | intron variant | G/T | snv | 9.2E-02 | 1 | ||
| rs11247735 | 1.000 | 0.080 | 1 | 25804968 | intron variant | G/A;C | snv | 1 | |||
| rs2072749 | 1.000 | 0.080 | 1 | 25804530 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs4659382 | 1.000 | 0.080 | 1 | 25808435 | intron variant | C/A;G | snv | 1 | |||
| rs718391 | 1.000 | 0.080 | 1 | 25799343 | upstream gene variant | C/G | snv | 0.54 | 1 | ||
| rs956304 | 1.000 | 0.080 | 17 | 30236544 | upstream gene variant | T/C | snv | 9.0E-03 | 1 | ||
| rs11718498 | 1.000 | 0.080 | 3 | 126654076 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs9637365 | 1.000 | 0.080 | 3 | 126651323 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs17268122 | 1.000 | 0.080 | 13 | 95192240 | intron variant | G/A;C;T | snv | 2 | |||
| rs2073438 | 0.925 | 0.160 | 17 | 6996757 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs2227935 | 0.925 | 0.080 | 15 | 90782869 | missense variant | C/A;G;T | snv | 4.0E-06; 5.6E-02 | 2 | ||
| rs4596 | 1.000 | 0.080 | 11 | 18366581 | 3 prime UTR variant | G/C | snv | 0.41 | 2 | ||
| rs2273626 | 0.925 | 0.120 | 14 | 22956973 | mature miRNA variant | C/A | snv | 0.58 | 0.41 | 2 | |
| rs10889675 | 1.000 | 0.080 | 1 | 67256533 | intron variant | C/A | snv | 0.11 | 2 | ||
| rs7542081 | 1.000 | 0.080 | 1 | 67237570 | intron variant | C/A | snv | 0.56 | 2 |