Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 25 | ||
rs115707823 | 0.701 | 0.320 | 6 | 30374976 | intergenic variant | G/A | snv | 19 | |||
rs7931342 | 0.689 | 0.360 | 11 | 69227030 | intergenic variant | T/G | snv | 0.58 | 19 | ||
rs11907546 | 0.708 | 0.280 | 20 | 34131991 | upstream gene variant | C/A;T | snv | 17 | |||
rs141752671 | 0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 | 17 | ||
rs147527678 | 0.708 | 0.280 | 6 | 32699696 | intergenic variant | G/A;C | snv | 17 | |||
rs147680653 | 0.708 | 0.280 | 6 | 29785031 | intergenic variant | A/G | snv | 17 | |||
rs148883465 | 0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 | 17 | ||
rs1862626 | 0.708 | 0.280 | 5 | 56737113 | regulatory region variant | G/T | snv | 0.68 | 17 | ||
rs186507655 | 0.708 | 0.280 | 1 | 1351675 | upstream gene variant | G/A | snv | 6.8E-03 | 17 | ||
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 4 | ||
rs3814113 | 0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 | 4 | ||
rs10962692 | 0.925 | 0.120 | 9 | 16915876 | upstream gene variant | G/A;C | snv | 3 | |||
rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 3 | ||
rs62274041 | 0.925 | 0.120 | 3 | 156717851 | upstream gene variant | G/A;T | snv | 3 | |||
rs4691139 | 1.000 | 0.120 | 4 | 164987569 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs67397200 | 0.827 | 0.160 | 19 | 17290595 | upstream gene variant | C/G | snv | 0.27 | 2 | ||
rs10674174 | 1.000 | 0.120 | 13 | 61317942 | intergenic variant | -/G | ins | 1 | |||
rs10899426 | 1.000 | 0.120 | 11 | 78008566 | intergenic variant | T/C | snv | 3.3E-02 | 1 | ||
rs111970895 | 1.000 | 0.120 | 5 | 102301953 | upstream gene variant | -/AAA;AAAAAA | delins | 1 | |||
rs12025262 | 1.000 | 0.120 | 1 | 247193430 | intron variant | G/A;C;T | snv | 1 | |||
rs12031579 | 1.000 | 0.120 | 1 | 119307920 | intron variant | G/A | snv | 6.8E-02 | 1 | ||
rs137672 | 1.000 | 0.120 | 22 | 39341089 | intergenic variant | C/T | snv | 0.40 | 1 | ||
rs144199732 | 1.000 | 0.120 | X | 43022624 | intergenic variant | C/T | snv | 1.2E-02 | 1 | ||
rs145065165 | 1.000 | 0.120 | 16 | 55347327 | intergenic variant | G/A | snv | 1.0E-03 | 1 |