Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10826548 | 1.000 | 0.040 | 10 | 28966665 | intergenic variant | C/A | snv | 0.13 | 1 | ||
rs114181198 | 1.000 | 0.040 | 2 | 183618431 | intergenic variant | C/A | snv | 1 | |||
rs11514810 | 1.000 | 0.040 | 7 | 1388840 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs11564750 | 1.000 | 0.040 | 5 | 1447647 | upstream gene variant | G/C;T | snv | 6.6E-02 | 1 | ||
rs12036759 | 1.000 | 0.040 | 1 | 232789695 | regulatory region variant | A/G;T | snv | 1 | |||
rs12042052 | 1.000 | 0.040 | 1 | 232799973 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs1330598 | 1.000 | 0.040 | 13 | 61358998 | regulatory region variant | T/A;C | snv | 1 | |||
rs142458453 | 1.000 | 0.040 | 12 | 31377392 | downstream gene variant | TAAATAAA/-;TAAA;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAA | delins | 1 | |||
rs1427829 | 1.000 | 0.040 | 12 | 89366967 | intron variant | A/G | snv | 0.46 | 1 | ||
rs1464807 | 1.000 | 0.040 | 7 | 96733032 | intergenic variant | G/A;T | snv | 1 | |||
rs1517484 | 1.000 | 0.040 | 2 | 225373194 | intergenic variant | C/T | snv | 0.45 | 1 | ||
rs1592757 | 1.000 | 0.040 | 5 | 104554297 | intron variant | G/C | snv | 0.29 | 1 | ||
rs1616905 | 1.000 | 0.040 | 13 | 90718584 | regulatory region variant | T/C | snv | 1 | |||
rs17058466 | 1.000 | 0.040 | 18 | 75893390 | intergenic variant | G/A | snv | 2.6E-02 | 1 | ||
rs200508662 | 1.000 | 0.040 | 5 | 121055487 | upstream gene variant | C/G;T | snv | 1 | |||
rs2410116 | 1.000 | 0.040 | 8 | 13815938 | intergenic variant | A/G;T | snv | 1 | |||
rs28600876 | 1.000 | 0.040 | 11 | 69890712 | intergenic variant | G/C | snv | 0.31 | 1 | ||
rs4075163 | 1.000 | 0.040 | 9 | 88984188 | intergenic variant | C/A | snv | 0.43 | 1 | ||
rs4858241 | 1.000 | 0.040 | 3 | 20627579 | intron variant | T/G | snv | 0.31 | 1 | ||
rs56135409 | 1.000 | 0.040 | 3 | 20683524 | intron variant | C/A | snv | 0.27 | 1 | ||
rs5906754 | 1.000 | 0.040 | X | 49203767 | upstream gene variant | C/T | snv | 0.51 | 1 | ||
rs6686722 | 1.000 | 0.040 | 1 | 175764827 | intergenic variant | C/G;T | snv | 1 | |||
rs7181782 | 1.000 | 0.040 | 15 | 80394651 | intron variant | C/A;G | snv | 1 | |||
rs726967 | 1.000 | 0.040 | 4 | 55555546 | downstream gene variant | A/T | snv | 0.28 | 1 | ||
rs7403703 | 1.000 | 0.040 | 15 | 87839033 | intergenic variant | A/G | snv | 0.49 | 1 |