| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs76661052 | 1.000 | 0.080 | 5 | 145379637 | intron variant | C/T | snv | 2.4E-02 | 1 | ||
| rs77530448 | 1.000 | 0.080 | 2 | 174729547 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs77777548 | 1.000 | 0.080 | 6 | 19628196 | intron variant | G/A | snv | 5.5E-03 | 1 | ||
| rs7843031 | 1.000 | 0.080 | 8 | 127521228 | intergenic variant | T/A;C | snv | 1 | |||
| rs7929962 | 1.000 | 0.080 | 11 | 69218116 | regulatory region variant | C/T | snv | 0.53 | 1 | ||
| rs8093601 | 1.000 | 0.080 | 18 | 54246103 | intergenic variant | G/C | snv | 0.40 | 1 | ||
| rs61415111 | 1.000 | 0.080 | 11 | 17399294 | intron variant | A/C | snv | 5.9E-04 | 1 | ||
| rs11859370 | 1.000 | 0.080 | 16 | 57619621 | intron variant | T/G | snv | 8.4E-02 | 1 | ||
| rs11863709 | 1.000 | 0.080 | 16 | 57620664 | intron variant | C/T | snv | 3.4E-02 | 1 | ||
| rs12480328 | 1.000 | 0.080 | 20 | 50911385 | intron variant | T/A;C;G | snv | 1 | |||
| rs60424486 | 1.000 | 0.080 | 7 | 15370686 | intron variant | -/TTTGAGAGGTGCCT | delins | 1 | |||
| rs17321482 | 1.000 | 0.080 | X | 11464514 | intron variant | C/T | snv | 9.0E-02 | 1 | ||
| rs2788524 | 1.000 | 0.080 | X | 11321091 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs12665339 | 1.000 | 0.080 | 6 | 30633455 | intron variant | A/G | snv | 0.13 | 1 | ||
| rs4906759 | 1.000 | 0.080 | 15 | 25730061 | intron variant | C/G;T | snv | 1 | |||
| rs4688181 | 1.000 | 0.080 | 3 | 64003780 | upstream gene variant | A/G | snv | 3.1E-02 | 1 | ||
| rs878987 | 1.000 | 0.080 | 11 | 134396478 | intron variant | A/G | snv | 0.16 | 1 | ||
| rs533722308 | 1.000 | 0.080 | 18 | 63293961 | intron variant | TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTTTT | delins | 1 | |||
| rs2842169 | 1.000 | 0.080 | 10 | 126642144 | intron variant | T/C | snv | 9.2E-02 | 1 | ||
| rs139882217 | 1.000 | 0.080 | 3 | 54695885 | intron variant | C/T | snv | 1.2E-02 | 1 | ||
| rs112193369 | 1.000 | 0.080 | 1 | 7498191 | intron variant | -/AGTGTG;AGTGTGTG;AGTGTTGGTG;AGTGTTGGTGTG;AGTGTTGGTGTGTG;GGTG | delins | 1 | |||
| rs17765344 | 1.000 | 0.080 | 17 | 71110733 | intron variant | A/G;T | snv | 1 | |||
| rs8071558 | 1.000 | 0.080 | 17 | 71111532 | intron variant | C/G;T | snv | 1 | |||
| rs138042437 | 1.000 | 0.080 | 8 | 127196124 | intron variant | A/G | snv | 4.0E-03 | 1 | ||
| rs1456305 | 1.000 | 0.080 | 8 | 127115007 | intron variant | G/A | snv | 0.88 | 1 |