Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
rs238406 | 0.677 | 0.480 | 19 | 45365051 | synonymous variant | T/G | snv | 0.58 | 0.65 | 23 | |
rs781049584 | 0.724 | 0.280 | 21 | 26021917 | missense variant | T/G | snv | 8.2E-06 | 7.0E-06 | 18 | |
rs12587 | 0.827 | 0.200 | 12 | 25205894 | 3 prime UTR variant | T/G | snv | 0.49 | 5 | ||
rs863225285 | 0.851 | 0.080 | 2 | 29209789 | missense variant | T/G | snv | 5 | |||
rs10162417 | 1.000 | 0.040 | 14 | 22460708 | intron variant | T/G | snv | 0.15 | 1 | ||
rs2191311 | 1.000 | 0.040 | 7 | 38295919 | non coding transcript exon variant | T/G | snv | 0.33 | 1 | ||
rs3811215 | 1.000 | 0.040 | 14 | 22485789 | upstream gene variant | T/G | snv | 0.80 | 1 | ||
rs3811244 | 1.000 | 0.040 | 14 | 22391078 | intron variant | T/G | snv | 0.35 | 1 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs1760944 | 0.672 | 0.480 | 14 | 20454990 | non coding transcript exon variant | T/C;G | snv | 26 | |||
rs1800975 | 0.701 | 0.360 | 9 | 97697296 | 5 prime UTR variant | T/C;G | snv | 0.63; 4.5E-06; 4.5E-06 | 19 | ||
rs1475170339 | 0.732 | 0.240 | 16 | 1792325 | missense variant | T/C;G | snv | 18 | |||
rs653765 | 0.763 | 0.240 | 15 | 58749813 | upstream gene variant | T/C;G | snv | 0.45 | 10 | ||
rs79977247 | 0.776 | 0.200 | 18 | 31592975 | missense variant | T/C;G | snv | 9 | |||
rs121912452 | 0.807 | 0.120 | 21 | 31667271 | missense variant | T/C;G | snv | 4.0E-06 | 6 | ||
rs4712653 | 0.882 | 0.080 | 6 | 22125735 | intron variant | T/C;G | snv | 3 | |||
rs765771575 | 0.882 | 0.080 | 7 | 116782017 | missense variant | T/C;G | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs34330 | 0.724 | 0.280 | 12 | 12717761 | 5 prime UTR variant | T/C | snv | 0.70 | 15 | ||
rs3136817 | 0.732 | 0.280 | 14 | 20456275 | intron variant | T/C | snv | 0.23 | 12 | ||
rs391957 | 0.763 | 0.240 | 9 | 125241745 | non coding transcript exon variant | T/C | snv | 0.72 | 10 | ||
rs35870237 | 0.763 | 0.120 | 12 | 40340404 | missense variant | T/C | snv | 9 |