Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 15 | |||
rs908832 | 0.851 | 0.120 | 9 | 137018032 | missense variant | A/C;G | snv | 0.97 | 0.96 | 4 | |
rs121908603 | 0.882 | 0.120 | 8 | 105802189 | missense variant | A/C;G | snv | 4.9E-04; 4.0E-06 | 3 | ||
rs2254638 | 0.882 | 0.040 | 21 | 28883961 | intron variant | A/C;G | snv | 3 | |||
rs2383205 | 0.925 | 0.080 | 9 | 22060936 | intron variant | A/C;G | snv | 3 | |||
rs879254920 | 0.882 | 0.120 | 19 | 11113665 | missense variant | A/C;G | snv | 3 | |||
rs2246942 | 0.925 | 0.040 | 10 | 89245129 | intron variant | A/C;G | snv | 2 | |||
rs1049007 | 1.000 | 0.040 | 20 | 6770387 | synonymous variant | A/C;G | snv | 0.67 | 1 | ||
rs12091564 | 1.000 | 0.040 | 1 | 146039391 | upstream gene variant | A/C;G | snv | 1 | |||
rs2281027 | 1.000 | 0.040 | 6 | 26446477 | intron variant | A/C;G | snv | 1 | |||
rs656451 | 1.000 | 0.040 | 16 | 77039597 | intergenic variant | A/C;G | snv | 2.4E-03 | 1 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
rs17465637 | 0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 | 11 | ||
rs10738609 | 1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv | 3 | |||
rs11881940 | 0.925 | 0.040 | 19 | 41302527 | non coding transcript exon variant | A/C;G;T | snv | 4.9E-06; 4.9E-06; 0.14 | 2 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs6505162 | 0.695 | 0.320 | 17 | 30117165 | 5 prime UTR variant | A/C;T | snv | 0.50; 3.1E-05 | 25 | ||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 21 | ||
rs1008438 | 0.807 | 0.120 | 6 | 31815431 | upstream gene variant | A/C;T | snv | 6 | |||
rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
rs2298566 | 0.827 | 0.040 | 11 | 130880747 | missense variant | A/C;T | snv | 0.77; 4.0E-06 | 5 |