Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs651821 | 0.851 | 0.360 | 11 | 116791863 | 5 prime UTR variant | C/T | snv | 0.88 | 0.89 | 10 | |
rs762679 | 8 | 47972876 | missense variant | T/A | snv | 0.87 | 0.88 | 4 | |||
rs8005100 | 14 | 58271048 | intron variant | A/C;G;T | snv | 0.69 | 1 | ||||
rs8012 | 19 | 12899706 | 3 prime UTR variant | A/G | snv | 0.61 | 0.64 | 2 | |||
rs1134634 | 4 | 15601446 | 3 prime UTR variant | G/C;T | snv | 0.58; 9.4E-06 | 2 | ||||
rs1264423 | 6 | 30603694 | non coding transcript exon variant | T/C | snv | 0.57 | 0.60 | 1 | |||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 17 | ||
rs4820268 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 5 | ||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 6 | ||
rs13108419 | 4 | 121766083 | non coding transcript exon variant | A/C;G | snv | 2.3E-05; 0.42 | 1 | ||||
rs56261297 | 8 | 143992685 | splice region variant | C/T | snv | 0.38 | 0.45 | 1 | |||
rs2278557 | 16 | 30082458 | intron variant | C/G | snv | 0.37 | 0.32 | 1 | |||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs2246434 | 1 | 158648665 | intron variant | G/A | snv | 0.26 | 0.22 | 1 | |||
rs742320 | 16 | 792706 | intron variant | G/A;C | snv | 0.25; 5.6E-06 | 1 | ||||
rs2942194 | 8 | 23566156 | missense variant | A/G | snv | 0.25 | 0.21 | 3 | |||
rs563995 | 19 | 43774629 | intron variant | G/A | snv | 0.24 | 0.34 | 3 | |||
rs1501466 | 11 | 2299654 | synonymous variant | A/G | snv | 0.19 | 0.22 | 1 | |||
rs2902548 | 10 | 102727625 | intron variant | C/T | snv | 0.18 | 0.20 | 1 | |||
rs652888 | 0.776 | 0.480 | 6 | 31883457 | non coding transcript exon variant | A/G | snv | 0.18 | 0.20 | 4 | |
rs3130618 | 0.827 | 0.360 | 6 | 31664357 | missense variant | C/A;T | snv | 0.15; 4.0E-06 | 1 | ||
rs2270927 | 5 | 76295885 | missense variant | C/A;G;T | snv | 0.14; 8.1E-06 | 1 | ||||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 | |||
rs6525433 | X | 70853309 | missense variant | T/C | snv | 0.12 | 0.14 | 1 |