Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10204525 | 0.701 | 0.440 | 2 | 241850169 | 3 prime UTR variant | C/T | snv | 0.21 | 20 | ||
rs10433937 | 0.882 | 0.080 | 4 | 87308948 | intron variant | T/A;C;G | snv | 4 | |||
rs104894630 | 0.882 | 0.120 | 17 | 10692805 | missense variant | G/A | snv | 4 | |||
rs1051861187 | 0.827 | 0.080 | 7 | 87409385 | missense variant | A/G | snv | 6 | |||
rs1053004 | 0.776 | 0.280 | 17 | 42314074 | 3 prime UTR variant | G/A | snv | 0.48 | 11 | ||
rs1053005 | 0.763 | 0.360 | 17 | 42313892 | 3 prime UTR variant | T/C | snv | 0.25 | 10 | ||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs10833 | 0.776 | 0.160 | 4 | 141733394 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 40 | ||
rs111200466 | 1.000 | 0.080 | 4 | 153684312 | 5 prime UTR variant | CGGCTGCTCGGCGTTCTCTCAGG/- | delins | 0.17 | 2 | ||
rs1137100 | 0.627 | 0.640 | 1 | 65570758 | missense variant | A/G | snv | 0.30 | 0.25 | 39 | |
rs11465817 | 0.882 | 0.120 | 1 | 67255414 | intron variant | C/A;T | snv | 4 | |||
rs11554495 | 0.701 | 0.240 | 12 | 52904798 | missense variant | C/A | snv | 4.9E-03 | 5.4E-03 | 19 | |
rs11881222 | 0.925 | 0.080 | 19 | 39244283 | intron variant | A/G | snv | 0.30 | 3 | ||
rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 22 | |
rs121434622 | 1.000 | 0.080 | X | 147936534 | missense variant | T/A | snv | 2 | |||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs12583006 | 0.807 | 0.320 | 13 | 108285104 | intron variant | T/A | snv | 0.21 | 8 | ||
rs1281032650 | 5 | 96979168 | missense variant | A/G | snv | 1 | |||||
rs1290547844 | 19 | 15273041 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs12980275 | 0.701 | 0.360 | 19 | 39241143 | upstream gene variant | A/G | snv | 0.36 | 23 | ||
rs1316569885 | 10 | 95399139 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |||
rs1325863623 | 6 | 2953175 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs1371149614 | 1.000 | 0.040 | 17 | 7630488 | missense variant | G/C | snv | 4.0E-06 | 2 |