Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17237820 | X | 116174483 | 3 prime UTR variant | A/T | snv | 5.7E-03 | 3 | ||||
rs6000582 | 22 | 37151454 | intron variant | G/T | snv | 3.8E-02 | 3 | ||||
rs8138057 | 22 | 37665537 | intron variant | G/A | snv | 3.0E-03 | 1.3E-02 | 6 | |||
rs9622186 | 22 | 35377961 | upstream gene variant | A/G | snv | 3.7E-03 | 6 | ||||
rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 6 | |||
rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 4 | ||
rs6065904 | 1.000 | 0.080 | 20 | 45906012 | intron variant | G/A | snv | 0.23 | 4 | ||
rs6065906 | 20 | 45925376 | downstream gene variant | T/A;C;G | snv | 4 | |||||
rs6073952 | 20 | 45908293 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs7679 | 0.925 | 0.160 | 20 | 45947863 | 3 prime UTR variant | T/C | snv | 0.13 | 6 | ||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 11 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 20 | |
rs2230667 | 19 | 49662445 | missense variant | C/T | snv | 1.0E-04 | 1.4E-05 | 6 | |||
rs33980385 | 19 | 40991388 | missense variant | A/G | snv | 6 | |||||
rs34338511 | 19 | 15184354 | missense variant | G/A;T | snv | 6.1E-04; 4.0E-06 | 3 | ||||
rs35980686 | 19 | 44757093 | missense variant | T/C | snv | 1.1E-03 | 4.4E-03 | 6 | |||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 15 | ||
rs11873890 | 18 | 662135 | intron variant | A/G | snv | 8.2E-03 | 3.2E-02 | 4 | |||
rs4987867 | 18 | 63123839 | 3 prime UTR variant | C/T | snv | 6.4E-03 | 3 | ||||
rs8086463 | 18 | 23532038 | 3 prime UTR variant | A/G | snv | 1.1E-02 | 3 | ||||
rs7212502 | 17 | 30222184 | intron variant | A/G | snv | 3.2E-02 | 3 | ||||
rs8071787 | 17 | 10058819 | intron variant | T/C | snv | 4.8E-02 | 5 | ||||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 9 | |||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 5 |