Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2695165 | 15 | 41781199 | intron variant | C/T | snv | 1.00 | 0.42 | 1 | |||
rs4758675 | 12 | 122207191 | missense variant | C/A;G | snv | 1.00 | 0.99 | 1 | |||
rs2797436 | 0.925 | 0.040 | 1 | 237700418 | synonymous variant | T/A;G | snv | 7.0E-05; 0.99 | 2 | ||
rs6670122 | 0.882 | 0.120 | 1 | 156737983 | intron variant | T/C;G | snv | 0.99 | 2 | ||
rs614754 | 6 | 160084167 | synonymous variant | C/G | snv | 0.99 | 0.99 | 1 | |||
rs690346 | 1.000 | 0.080 | 15 | 53716648 | missense variant | T/C | snv | 0.99 | 0.96 | 1 | |
rs6736913 | 1.000 | 0.040 | 2 | 42282878 | stop gained | A/G;T | snv | 0.99 | 1 | ||
rs4387351 | 1.000 | 0.040 | 11 | 62613260 | 5 prime UTR variant | T/C | snv | 0.98 | 0.94 | 2 | |
rs105633 | 0.882 | 0.040 | 5 | 141945684 | synonymous variant | T/C;G | snv | 0.98; 4.0E-06 | 3 | ||
rs6050446 | 20 | 25214873 | stop gained | A/G;T | snv | 0.98 | 1 | ||||
rs1144566 | 1 | 182600491 | missense variant | T/A;C;G | snv | 0.98 | 1 | ||||
rs2664521 | 20 | 48636612 | stop gained | T/A;C | snv | 0.98 | 1 | ||||
rs1013579 | 1 | 56956811 | missense variant | C/T | snv | 0.98 | 0.98 | 1 | |||
rs1435547 | 1.000 | 0.080 | 2 | 11597965 | missense variant | T/A;C | snv | 0.98 | 1 | ||
rs3744644 | 1.000 | 0.080 | 17 | 1635334 | missense variant | C/A;G | snv | 1.6E-05; 0.97 | 1 | ||
rs428113 | 1.000 | 0.040 | 19 | 2991816 | intron variant | T/A;C;G | snv | 0.97; 4.0E-06 | 1 | ||
rs6472812 | 1.000 | 0.080 | 8 | 74004849 | missense variant | A/G | snv | 0.97 | 0.97 | 1 | |
rs12147030 | 1.000 | 0.040 | 14 | 89401634 | missense variant | T/C | snv | 0.97 | 0.93 | 1 | |
rs7105056 | 11 | 112193708 | non coding transcript exon variant | T/C | snv | 0.97 | 0.95 | 1 | |||
rs643507 | 1.000 | 0.080 | 18 | 2946293 | non coding transcript exon variant | C/T | snv | 0.96 | 0.92 | 1 | |
rs908830 | 9 | 136946407 | intron variant | T/C | snv | 0.96 | 0.95 | 1 | |||
rs10283100 | 8 | 119583783 | missense variant | A/G;T | snv | 0.96 | 3 | ||||
rs299163 | 19 | 55810048 | missense variant | C/A;T | snv | 0.96 | 1 | ||||
rs758386 | 3 | 45775926 | stop gained | A/G;T | snv | 0.96 | 1 | ||||
rs6784615 | 1.000 | 0.080 | 3 | 52472410 | intron variant | C/T | snv | 0.96 | 0.96 | 1 |