Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 7 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 5 | |||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs4432538 | 20 | 8626746 | intron variant | G/A | snv | 0.52 | 4 | ||||
rs8176685 | 9 | 133263363 | intron variant | CACCACTACGCC/- | delins | 4 | |||||
rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 | ||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 3 | |||||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 3 | ||
rs12445050 | 16 | 81837364 | intron variant | C/T | snv | 9.6E-02 | 3 | ||||
rs139141690 | 7 | 101856650 | intron variant | G/A | snv | 2.2E-03 | 3 | ||||
rs3804749 | 3 | 123114156 | intron variant | C/T | snv | 0.48 | 3 | ||||
rs41315846 | 1 | 247549001 | intron variant | T/C | snv | 0.44 | 0.52 | 3 | |||
rs4907622 | 13 | 113362571 | intron variant | G/C;T | snv | 3 | |||||
rs655029 | 2 | 31254972 | intron variant | G/A | snv | 0.78 | 3 | ||||
rs7641175 | 3 | 18269920 | intron variant | G/A | snv | 0.81 | 3 | ||||
rs10840293 | 1.000 | 0.040 | 11 | 9729649 | intron variant | G/A;C | snv | 2 | |||
rs11030122 | 11 | 3865946 | intron variant | C/G | snv | 0.27 | 2 | ||||
rs11083766 | 19 | 45212232 | intron variant | T/C | snv | 0.26 | 2 | ||||
rs11121012 | 1 | 7734229 | intron variant | A/G | snv | 0.62 | 2 | ||||
rs111941366 | 1 | 25409878 | intron variant | C/T | snv | 0.30 | 2 | ||||
rs11653357 | 17 | 35596588 | intron variant | G/A;C | snv | 2 | |||||
rs17708984 | 19 | 16083694 | intron variant | G/A | snv | 0.27 | 2 |