Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs146425640 | 1.000 | 11 | 19823052 | intron variant | A/C | snv | 2.8E-03 | 1 | |||
rs184429573 | 1.000 | 12 | 28504235 | intron variant | A/C | snv | 9.1E-03 | 1 | |||
rs190508378 | 1.000 | 21 | 31697608 | intron variant | A/C | snv | 3.4E-03 | 1 | |||
rs57997684 | 1.000 | 6 | 11014323 | intron variant | A/C | snv | 0.13 | 1 | |||
rs73184656 | 1.000 | 3 | 187724028 | intron variant | A/C | snv | 0.18 | 1 | |||
rs4767831 | 1.000 | 12 | 119601623 | intron variant | A/C;G | snv | 1 | ||||
rs10505380 | 1.000 | 8 | 120314234 | intron variant | A/G | snv | 0.14 | 1 | |||
rs67134687 | 1.000 | 9 | 21845309 | intron variant | A/G | snv | 9.2E-02 | 1 | |||
rs7048567 | 1.000 | 9 | 137009585 | synonymous variant | A/G | snv | 0.68 | 0.70 | 1 | ||
rs75495219 | 1.000 | 10 | 67151138 | intron variant | A/G | snv | 6.0E-02 | 1 | |||
rs1882642 | 1.000 | 2 | 141104341 | intron variant | A/G;T | snv | 1 | ||||
rs117451620 | 1.000 | 22 | 33873469 | intron variant | C/A | snv | 1.8E-02 | 1 | |||
rs76456255 | 1.000 | 12 | 65950114 | intron variant | C/A | snv | 6.5E-02 | 1 | |||
rs139465532 | 1.000 | 20 | 8348184 | intron variant | C/G | snv | 6.8E-03 | 1 | |||
rs142630661 | 1.000 | 11 | 71794579 | non coding transcript exon variant | C/G | snv | 1.3E-02 | 1 | |||
rs189131320 | 1.000 | 1 | 24951485 | intron variant | C/G | snv | 2.3E-03 | 1 | |||
rs114830967 | 1.000 | 2 | 115820465 | intron variant | C/T | snv | 2.0E-02 | 1 | |||
rs12118495 | 1.000 | 1 | 204077651 | intron variant | C/T | snv | 7.8E-02 | 1 | |||
rs12232685 | 1.000 | 18 | 13437028 | intron variant | C/T | snv | 4.8E-02 | 1 | |||
rs140255439 | 1.000 | 17 | 2638960 | intron variant | C/T | snv | 6.3E-02 | 1 | |||
rs142897541 | 1.000 | 2 | 192095144 | intron variant | C/T | snv | 1.6E-02 | 1 | |||
rs150859230 | 1.000 | 1 | 216675108 | intron variant | C/T | snv | 1.4E-02 | 1 | |||
rs151068302 | 1.000 | 9 | 26883048 | intron variant | C/T | snv | 6.1E-02 | 1 | |||
rs192597095 | 1.000 | 12 | 56486375 | intron variant | C/T | snv | 8.6E-03 | 1 | |||
rs72656469 | 1.000 | 8 | 64701356 | intron variant | C/T | snv | 1.9E-02 | 1 |