Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs2472297 | 0.882 | 0.160 | 15 | 74735539 | intergenic variant | C/T | snv | 0.16 | 9 | ||
rs4410790 | 0.882 | 0.160 | 7 | 17244953 | intron variant | T/C | snv | 0.54 | 9 | ||
rs784257 | 1.000 | 0.080 | 18 | 55729968 | intron variant | T/A;C | snv | 4 | |||
rs17046344 | 2 | 54796463 | intron variant | G/A | snv | 0.11 | 3 | ||||
rs588321 | 11 | 1875727 | intron variant | G/C;T | snv | 3 | |||||
rs36096257 | 2 | 121281207 | missense variant | G/A | snv | 6.8E-03 | 2.9E-03 | 3 | |||
rs7215775 | 17 | 61406955 | non coding transcript exon variant | A/G | snv | 0.68 | 2 | ||||
rs7495833 | 15 | 53651121 | intron variant | C/A | snv | 0.37 | 2 | ||||
rs12037987 | 1 | 112500200 | intron variant | T/C | snv | 8.6E-02 | 2 | ||||
rs1290083 | 15 | 50858717 | intron variant | T/A;C | snv | 1 | |||||
rs12944041 | 17 | 8169779 | downstream gene variant | G/A | snv | 0.42 | 1 | ||||
rs13143189 | 4 | 3755653 | downstream gene variant | G/A | snv | 0.36 | 1 | ||||
rs254023 | 5 | 104619660 | intron variant | T/C | snv | 0.43 | 1 | ||||
rs4973766 | 3 | 27372075 | intron variant | C/T | snv | 0.38 | 1 | ||||
rs6647951 | X | 76165707 | intergenic variant | C/T | snv | 2.2E-02 | 1 | ||||
rs72704791 | 5 | 547781 | intergenic variant | A/G | snv | 0.14 | 1 | ||||
rs6467447 | 7 | 132840387 | intron variant | C/T | snv | 0.69 | 1 | ||||
rs12465752 | 2 | 121355564 | intron variant | C/T | snv | 0.12 | 1 | ||||
rs10854166 | 19 | 18542034 | 5 prime UTR variant | A/G | snv | 0.46 | 0.37 | 1 | |||
rs929250 | 7 | 27205482 | non coding transcript exon variant | G/T | snv | 0.93 | 1 | ||||
rs1275980 | 2 | 26694101 | intron variant | C/T | snv | 0.48 | 1 | ||||
rs5912570 | X | 78218174 | intergenic variant | C/T | snv | 0.45 | 1 | ||||
rs61375854 | 6 | 54681503 | intergenic variant | T/G | snv | 0.40 | 1 | ||||
rs118070237 | 16 | 56795510 | intron variant | T/C | snv | 4.7E-04 | 1 |