Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2468024 | 8 | 97652425 | intron variant | G/A;C | snv | 3 | |||||
rs2492301 | 1 | 37473572 | intron variant | T/C | snv | 0.53 | 4 | ||||
rs2537594 | 7 | 17774912 | intergenic variant | G/A | snv | 0.58 | 3 | ||||
rs2834259 | 21 | 33760786 | intron variant | C/T | snv | 0.30 | 3 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 5 | ||||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs3208787 | 17 | 81558634 | 3 prime UTR variant | A/G | snv | 0.24 | 4 | ||||
rs34536858 | 19 | 35459272 | intergenic variant | A/G | snv | 0.33 | 3 | ||||
rs35158985 | 0.882 | 0.080 | 16 | 68762843 | intron variant | A/G | snv | 0.38 | 6 | ||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs35893164 | 6 | 37175357 | 3 prime UTR variant | A/G | snv | 6.5E-03 | 4 | ||||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs3740685 | 11 | 47447239 | intron variant | C/T | snv | 0.59 | 3 | ||||
rs3756668 | 0.925 | 0.160 | 5 | 68300260 | 3 prime UTR variant | G/A;C | snv | 5 | |||
rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
rs4332427 | 10 | 24569461 | intergenic variant | A/G | snv | 0.21 | 3 | ||||
rs532591337 | 19 | 12459271 | intron variant | G/A | snv | 4.9E-05 | 4 | ||||
rs55709272 | 2 | 113109711 | intron variant | T/A;C | snv | 5 | |||||
rs56129102 | 13 | 113220766 | intron variant | C/T | snv | 0.20 | 3 | ||||
rs57565032 | 12 | 131949846 | upstream gene variant | G/T | snv | 0.14 | 4 | ||||
rs58658771 | 0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 | 13 | ||
rs6000550 | 22 | 37067410 | intron variant | C/G;T | snv | 0.21 | 4 | ||||
rs6014993 | 20 | 57416581 | regulatory region variant | A/G | snv | 0.58 | 5 | ||||
rs6068729 | 20 | 53931121 | intergenic variant | C/T | snv | 0.19 | 3 | ||||
rs6084653 | 20 | 4176425 | intron variant | C/G;T | snv | 3 |