Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2857656 | 0.851 | 0.120 | 17 | 34254988 | upstream gene variant | G/A;C | snv | 5 | |||
rs4957796 | 0.851 | 0.120 | 5 | 109066439 | intron variant | T/C | snv | 0.16 | 5 | ||
rs17446614 | 0.851 | 0.240 | 13 | 40565740 | intron variant | G/A | snv | 0.16 | 5 | ||
rs2232618 | 0.851 | 0.160 | 20 | 38373117 | missense variant | T/C | snv | 9.2E-02 | 0.12 | 5 | |
rs9770242 | 0.851 | 0.240 | 7 | 106285885 | 5 prime UTR variant | C/A | snv | 0.79 | 5 | ||
rs2069948 | 0.851 | 0.160 | 20 | 35174686 | non coding transcript exon variant | C/T | snv | 0.55 | 0.62 | 5 | |
rs2234246 | 0.827 | 0.240 | 6 | 41276002 | 3 prime UTR variant | C/T | snv | 0.44 | 5 | ||
rs13137 | 0.827 | 0.160 | 17 | 59841670 | 3 prime UTR variant | A/T | snv | 0.18 | 5 | ||
rs353291 | 0.807 | 0.200 | 5 | 149431183 | non coding transcript exon variant | T/C | snv | 0.35 | 6 | ||
rs2297630 | 0.827 | 0.160 | 10 | 44376100 | intron variant | G/A;T | snv | 0.21 | 6 | ||
rs41274221 | 0.851 | 0.160 | 7 | 100093577 | mature miRNA variant | C/T | snv | 6.4E-05 | 4.9E-05 | 6 | |
rs842647 | 0.827 | 0.400 | 2 | 60892336 | intron variant | G/A | snv | 0.62 | 6 | ||
rs1799768 | 0.807 | 0.360 | 7 | 101126425 | upstream gene variant | -/A;C | ins | 6 | |||
rs4358188 | 0.827 | 0.160 | 20 | 38318446 | missense variant | G/A;C | snv | 0.46 | 7 | ||
rs11465996 | 0.790 | 0.240 | 8 | 73989727 | upstream gene variant | C/G | snv | 0.25 | 7 | ||
rs1126647 | 0.827 | 0.160 | 4 | 73743328 | 3 prime UTR variant | A/T | snv | 0.31 | 8 | ||
rs212388 | 0.827 | 0.240 | 6 | 159069404 | intron variant | C/G;T | snv | 8 | |||
rs121918094 | 0.827 | 0.280 | 18 | 31592921 | missense variant | T/C | snv | 8 | |||
rs414171 | 0.790 | 0.200 | 3 | 50612068 | 5 prime UTR variant | A/G;T | snv | 9 | |||
rs4648068 | 0.790 | 0.240 | 4 | 102597148 | intron variant | A/G | snv | 0.31 | 9 | ||
rs2234237 | 0.763 | 0.280 | 6 | 41282728 | missense variant | T/A | snv | 0.13 | 0.12 | 9 | |
rs653765 | 0.763 | 0.240 | 15 | 58749813 | upstream gene variant | T/C;G | snv | 0.45 | 10 | ||
rs1143643 | 0.790 | 0.320 | 2 | 112830725 | intron variant | C/T | snv | 0.29 | 10 | ||
rs11568821 | 0.827 | 0.200 | 2 | 241851760 | intron variant | C/G;T | snv | 10 | |||
rs510432 | 0.752 | 0.280 | 6 | 106326155 | upstream gene variant | T/C | snv | 0.57 | 11 |