Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2235573 | 0.882 | 0.040 | 22 | 38081923 | synonymous variant | G/A | snv | 0.47 | 0.46 | 4 | |
rs6519265 | 1.000 | 0.040 | 22 | 41629346 | intron variant | A/G | snv | 1 | |||
rs1034749666 | 0.776 | 0.160 | 21 | 33027257 | missense variant | G/A | snv | 9 | |||
rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 21 | |||
rs2297440 | 0.763 | 0.080 | 20 | 63680946 | intron variant | T/C | snv | 0.81 | 10 | ||
rs4809324 | 0.807 | 0.200 | 20 | 63686867 | non coding transcript exon variant | T/C | snv | 8.8E-02 | 7 | ||
rs6062302 | 0.882 | 0.040 | 20 | 63689615 | synonymous variant | T/C | snv | 0.74 | 0.81 | 4 | |
rs1058319 | 1.000 | 0.040 | 20 | 63743036 | 3 prime UTR variant | C/A;T | snv | 0.21 | 2 | ||
rs2236507 | 1.000 | 0.040 | 20 | 63691653 | intron variant | G/C;T | snv | 2 | |||
rs115303435 | 1.000 | 0.040 | 20 | 63694806 | missense variant | G/A | snv | 3.2E-03 | 1.1E-03 | 1 | |
rs3761121 | 1.000 | 0.040 | 20 | 63711343 | intron variant | T/C | snv | 0.10 | 1 | ||
rs5019252 | 1.000 | 0.040 | 20 | 63746996 | synonymous variant | C/T | snv | 0.34 | 0.30 | 1 | |
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 | |
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs25489 | 0.550 | 0.720 | 19 | 43552260 | missense variant | C/G;T | snv | 8.5E-06; 7.1E-02 | 78 | ||
rs1799793 | 0.557 | 0.640 | 19 | 45364001 | missense variant | C/A;T | snv | 7.1E-06; 0.29 | 72 | ||
rs11615 | 0.572 | 0.640 | 19 | 45420395 | synonymous variant | A/G | snv | 0.50 | 0.55 | 62 | |
rs3212986 | 0.620 | 0.400 | 19 | 45409478 | stop gained | C/A;G;T | snv | 0.29; 4.3E-06; 4.3E-06 | 42 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs2298881 | 0.653 | 0.400 | 19 | 45423658 | intron variant | C/A;T | snv | 25 | |||
rs3787016 | 0.677 | 0.280 | 19 | 1090804 | intron variant | A/G | snv | 0.78 | 24 | ||
rs1214285376 | 0.776 | 0.200 | 19 | 43543490 | missense variant | G/T | snv | 4.0E-06 | 8 | ||
rs148611340 | 0.790 | 0.120 | 19 | 43543621 | missense variant | G/A;C | snv | 4.0E-06; 1.2E-05 | 7 | ||
rs199613843 | 0.807 | 0.160 | 19 | 43551609 | synonymous variant | C/T | snv | 4.0E-06 | 7.0E-06 | 6 |