Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 35 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 19 | ||
rs5744680 | 0.851 | 0.120 | 5 | 75584065 | intron variant | G/A | snv | 0.55 | 18 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 17 | |||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 17 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 13 | ||
rs58658771 | 0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 | 13 | ||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 13 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 12 |