Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs533450458 | 0.925 | 0.120 | 8 | 90042781 | missense variant | C/T | snv | 5.5E-04 | 7.7E-05 | 2 | |
rs9989419 | 0.882 | 0.120 | 16 | 56951227 | regulatory region variant | A/G | snv | 0.55 | 11 | ||
rs11572103 | 0.851 | 0.120 | 10 | 95058349 | missense variant | T/A | snv | 1.6E-02 | 4.9E-02 | 4 | |
rs1223493898 | 0.851 | 0.120 | 20 | 44406090 | missense variant | G/A;C | snv | 5 | |||
rs1408888 | 0.851 | 0.120 | 13 | 71854515 | intron variant | T/G | snv | 0.30 | 5 | ||
rs2518136 | 0.851 | 0.120 | 3 | 186620038 | intron variant | T/C | snv | 0.46 | 4 | ||
rs7212 | 0.851 | 0.120 | 1 | 145992816 | 3 prime UTR variant | G/C | snv | 0.16 | 5 | ||
rs805296 | 0.851 | 0.120 | 6 | 31655116 | intron variant | T/A;C | snv | 4 | |||
rs10757283 | 0.827 | 0.120 | 9 | 22134173 | intergenic variant | C/A;T | snv | 0.45 | 6 | ||
rs12050217 | 0.827 | 0.160 | 14 | 96262416 | intron variant | A/G | snv | 0.21 | 6 | ||
rs3088442 | 0.827 | 0.120 | 6 | 160451620 | 3 prime UTR variant | G/A | snv | 0.28 | 5 | ||
rs6700896 | 0.827 | 0.160 | 1 | 65624099 | intron variant | C/T | snv | 0.44 | 9 | ||
rs9289231 | 0.827 | 0.120 | 3 | 124055231 | intergenic variant | T/G | snv | 0.15 | 5 | ||
rs10911021 | 0.807 | 0.160 | 1 | 182112825 | intron variant | C/T | snv | 0.36 | 11 | ||
rs1282382243 | 0.807 | 0.120 | 13 | 50843630 | missense variant | G/A | snv | 8 | |||
rs17366743 | 0.807 | 0.280 | 3 | 186854300 | missense variant | T/C | snv | 2.2E-02 | 2.1E-02 | 7 | |
rs5082 | 0.807 | 0.160 | 1 | 161223893 | upstream gene variant | G/A | snv | 0.68 | 8 | ||
rs775381348 | 0.807 | 0.160 | 14 | 35308023 | missense variant | G/T | snv | 8 | |||
rs9267551 | 0.807 | 0.160 | 6 | 31730180 | 5 prime UTR variant | C/G;T | snv | 7 | |||
rs146292819 | 0.790 | 0.240 | 9 | 104794495 | missense variant | T/G | snv | 2.9E-04 | 3.8E-04 | 9 | |
rs16933090 | 0.790 | 0.160 | 11 | 16434247 | 5 prime UTR variant | C/T | snv | 0.12 | 7 | ||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 18 | ||
rs2297508 | 0.790 | 0.240 | 17 | 17812003 | synonymous variant | C/G;T | snv | 0.50; 7.5E-05 | 8 | ||
rs3732581 | 0.790 | 0.120 | 3 | 183840614 | missense variant | C/G;T | snv | 0.46; 1.2E-05 | 9 | ||
rs6850 | 0.790 | 0.160 | 7 | 44796715 | 5 prime UTR variant | A/G;T | snv | 0.26; 4.0E-06 | 9 |