Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11655237 | 0.724 | 0.280 | 17 | 72404025 | non coding transcript exon variant | C/T | snv | 0.16 | 17 | ||
rs12108497 | 0.851 | 0.080 | 4 | 184650403 | intron variant | C/G;T | snv | 6 | |||
rs121434568 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 73 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 135 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 60 | ||
rs12416605 | 0.925 | 0.080 | 10 | 29602331 | mature miRNA variant | C/T | snv | 0.22 | 0.20 | 3 | |
rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
rs12826786 | 0.683 | 0.480 | 12 | 53961717 | upstream gene variant | C/T | snv | 0.38 | 26 | ||
rs12917 | 0.605 | 0.480 | 10 | 129708019 | missense variant | C/T | snv | 0.14 | 0.14 | 45 | |
rs13042395 | 0.752 | 0.160 | 20 | 773867 | intron variant | C/T | snv | 5.9E-02 | 13 | ||
rs1305398818 | 0.925 | 0.080 | 4 | 88131886 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs13252298 | 0.827 | 0.160 | 8 | 127082911 | non coding transcript exon variant | A/G | snv | 0.24 | 7 | ||
rs13361707 | 0.882 | 0.120 | 5 | 40791782 | intron variant | C/T | snv | 0.31 | 6 | ||
rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
rs13428812 | 0.827 | 0.120 | 2 | 25269598 | intron variant | A/G | snv | 0.31 | 8 | ||
rs1353702185 | 0.550 | 0.720 | 12 | 68839311 | missense variant | C/G | snv | 4.0E-06 | 79 | ||
rs1447295 | 0.658 | 0.400 | 8 | 127472793 | intron variant | A/C;T | snv | 28 | |||
rs144779807 | 0.827 | 0.120 | 5 | 1268529 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-05 | 7 | ||
rs1458766475 | 0.637 | 0.680 | 1 | 169732649 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 41 | ||
rs1468063 | 0.851 | 0.200 | 10 | 89015534 | 3 prime UTR variant | C/T | snv | 0.17 | 0.17 | 6 | |
rs148704956 | 0.716 | 0.360 | 6 | 52187772 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 19 | |
rs1520220 | 0.807 | 0.280 | 12 | 102402744 | intron variant | G/C;T | snv | 0.76 | 9 | ||
rs1550117 | 0.790 | 0.320 | 2 | 25343038 | upstream gene variant | A/G;T | snv | 11 |