Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs10233018 | 0.925 | 0.040 | 7 | 117883655 | non coding transcript exon variant | A/G | snv | 0.53 | 2 | ||
rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
rs10485715 | 0.925 | 0.040 | 20 | 7279278 | intergenic variant | T/C | snv | 5.5E-02 | 2 | ||
rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 1 | ||
rs10809520 | 0.925 | 0.040 | 9 | 11557797 | intergenic variant | C/T | snv | 0.28 | 2 | ||
rs10884216 | 0.925 | 0.040 | 10 | 105701367 | intergenic variant | T/C | snv | 0.17 | 2 | ||
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 2 | ||
rs11082011 | 0.925 | 0.040 | 18 | 37565159 | intron variant | C/T | snv | 0.53 | 3 | ||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
rs11155372 | 0.925 | 0.040 | 6 | 144698602 | intron variant | G/C;T | snv | 3 | |||
rs112106319 | 0.925 | 0.040 | 9 | 115094539 | intron variant | A/T | snv | 2.8E-03 | 3 | ||
rs112538845 | 0.925 | 0.040 | 4 | 184084475 | downstream gene variant | C/T | snv | 1.7E-02 | 3 | ||
rs11591827 | 0.925 | 0.040 | 10 | 81128126 | intergenic variant | G/A | snv | 8.4E-02 | 3 | ||
rs116609693 | 0.925 | 0.040 | 9 | 92811394 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs11728985 | 0.925 | 0.040 | 4 | 129115280 | 3 prime UTR variant | C/T | snv | 0.12 | 3 | ||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs11924809 | 0.925 | 0.040 | 3 | 186353656 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
rs11990063 | 0.925 | 0.040 | 8 | 10307685 | intron variant | C/A;T | snv | 3 | |||
rs120074175 | 0.827 | 0.080 | 12 | 72031544 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs12555870 | 0.925 | 0.040 | 9 | 23347726 | intron variant | A/G | snv | 0.36 | 3 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 1 | |||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 |