Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs148910659 | 17 | 46055293 | intron variant | G/A | snv | 3 | |||||
rs78746179 | 17 | 46127240 | intron variant | C/T | snv | 5.0E-02 | 2 | ||||
rs35524223 | 17 | 46115224 | intron variant | T/A | snv | 0.14 | 2 | ||||
rs776509440 | 17 | 46096136 | intron variant | -/CTT;CTTT;CTTTT;CTTTTT;CTTTTTT;CTTTTTTT;CTTTTTTTT;CTTTTTTTTTT;CTTTTTTTTTTTTTTT | delins | 2 | |||||
rs11654745 | 17 | 46053730 | intron variant | G/A | snv | 0.35 | 2 | ||||
rs2696579 | 17 | 46150027 | intron variant | T/A;C | snv | 2 | |||||
rs142920272 | 17 | 46224474 | intron variant | T/A;C | snv | 1 | |||||
rs8080583 | 17 | 46085231 | intron variant | C/A | snv | 0.23 | 1 | ||||
rs4606752 | 17 | 46115252 | intron variant | A/G | snv | 0.14 | 1 | ||||
rs115231027 | 17 | 46121924 | intron variant | T/C | snv | 1 | |||||
rs11653367 | 17 | 46114117 | intron variant | A/G;T | snv | 1 | |||||
rs201408539 | 0.827 | 0.080 | 17 | 46088713 | intron variant | TA/- | delins | 6 | |||
rs7225002 | 0.925 | 0.080 | 17 | 46111701 | intron variant | A/G | snv | 0.39 | 5 | ||
rs2532263 | 1.000 | 0.080 | 17 | 46175102 | intron variant | G/A | snv | 0.12 | 1 | ||
rs17577094 | 0.925 | 0.120 | 17 | 46110126 | intron variant | A/G | snv | 0.14 | 1 |