Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10001106 | 0.925 | 0.120 | 4 | 10125817 | intergenic variant | T/A;C | snv | 3 | |||
rs10001964 | 0.925 | 0.120 | 4 | 9957651 | intron variant | C/T | snv | 0.48 | 3 | ||
rs10003001 | 0.925 | 0.120 | 4 | 9982851 | intron variant | C/T | snv | 0.21 | 3 | ||
rs10003864 | 0.925 | 0.120 | 4 | 10435767 | downstream gene variant | T/C | snv | 0.29 | 3 | ||
rs10006397 | 0.925 | 0.120 | 4 | 10034516 | non coding transcript exon variant | C/A | snv | 0.78 | 3 | ||
rs1000791 | 17 | 79269796 | intron variant | T/A | snv | 8.2E-02 | 1 | ||||
rs10008035 | 0.925 | 0.120 | 4 | 9997711 | intron variant | G/A;T | snv | 3 | |||
rs10009493 | 0.925 | 0.120 | 4 | 10130423 | intergenic variant | C/G | snv | 0.18 | 3 | ||
rs10009618 | 0.925 | 0.120 | 4 | 88172856 | intron variant | C/T | snv | 0.58 | 3 | ||
rs10010656 | 0.925 | 0.120 | 4 | 10244703 | intergenic variant | G/C | snv | 0.30 | 3 | ||
rs10011206 | 0.925 | 0.120 | 4 | 9990331 | intron variant | C/T | snv | 0.23 | 3 | ||
rs10011796 | 0.882 | 0.160 | 4 | 88169725 | intron variant | T/C;G | snv | 4 | |||
rs1001216 | 0.925 | 0.120 | 4 | 10167225 | non coding transcript exon variant | A/G | snv | 0.15 | 3 | ||
rs1001217 | 0.925 | 0.120 | 4 | 10167375 | non coding transcript exon variant | C/A;G | snv | 3 | |||
rs10012288 | 0.925 | 0.120 | 4 | 10139329 | downstream gene variant | G/A | snv | 0.42 | 3 | ||
rs10012779 | 0.925 | 0.120 | 4 | 10036488 | intron variant | C/T | snv | 0.15 | 3 | ||
rs10015494 | 0.925 | 0.120 | 4 | 10140366 | downstream gene variant | G/A;C;T | snv | 3 | |||
rs10015872 | 0.925 | 0.120 | 4 | 10140786 | downstream gene variant | G/A | snv | 0.42 | 3 | ||
rs10016022 | 0.925 | 0.120 | 4 | 10445282 | missense variant | A/G;T | snv | 0.74 | 3 | ||
rs10017305 | 0.925 | 0.120 | 4 | 10399599 | intergenic variant | T/C | snv | 0.26 | 3 | ||
rs10017447 | 0.925 | 0.120 | 4 | 10173912 | regulatory region variant | C/A | snv | 0.67 | 3 | ||
rs10017674 | 0.925 | 0.120 | 4 | 9965429 | intron variant | T/C | snv | 0.49 | 3 | ||
rs10018204 | 0.925 | 0.120 | 4 | 9962946 | intron variant | C/T | snv | 0.49 | 3 | ||
rs10020887 | 0.925 | 0.120 | 4 | 10139127 | downstream gene variant | C/A;G | snv | 3 | |||
rs10022499 | 0.925 | 0.120 | 4 | 10004913 | intron variant | C/A | snv | 0.72 | 3 |