Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10189761 | 0.882 | 0.120 | 2 | 646364 | intergenic variant | T/A | snv | 0.82 | 4 | ||
rs1022113606 | 0.732 | 0.280 | 4 | 24800161 | missense variant | G/C | snv | 1.6E-04 | 2.1E-05 | 17 | |
rs1028728 | 0.925 | 0.040 | 13 | 37599679 | upstream gene variant | A/T | snv | 0.20 | 3 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 25 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 12 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs10501920 | 0.882 | 0.080 | 11 | 99622442 | intron variant | C/G | snv | 0.14 | 3 | ||
rs10519210 | 1.000 | 0.040 | 15 | 63445726 | intergenic variant | T/C;G | snv | 1 | |||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 | ||
rs10932374 | 0.925 | 0.040 | 2 | 211379678 | 3 prime UTR variant | G/A | snv | 0.23 | 2 | ||
rs11006544 | 1.000 | 0.040 | 10 | 59510886 | intergenic variant | T/C | snv | 7.3E-03 | 3 | ||
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 | ||
rs11110004 | 1.000 | 0.040 | 12 | 99694540 | intron variant | T/C | snv | 5.1E-03 | 3 | ||
rs11172782 | 1.000 | 0.040 | 12 | 58865846 | intergenic variant | A/G | snv | 0.12 | 1 | ||
rs112434206 | 1.000 | 0.040 | 5 | 33083283 | intron variant | A/C;G | snv | 7.6E-03 | 3 | ||
rs113235453 | 1.000 | 0.040 | 14 | 31849939 | intron variant | A/G | snv | 3.5E-02 | 3 | ||
rs1136201 | 0.645 | 0.280 | 17 | 39723335 | missense variant | A/G;T | snv | 0.20 | 34 | ||
rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
rs114821210 | 1.000 | 0.040 | 5 | 166089843 | intergenic variant | C/A | snv | 6.0E-03 | 3 | ||
rs121918080 | 0.827 | 0.240 | 18 | 31595128 | missense variant | G/A;T | snv | 2.4E-05 | 6 | ||
rs121918090 | 0.790 | 0.240 | 18 | 31593026 | missense variant | G/C | snv | 8 |