Source: INFERRED ×
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 | 64 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 43 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 38 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 36 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 28 | |
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 25 | |
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 25 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 23 | ||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 23 | ||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 22 | ||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 22 | ||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 22 | |
rs247617 | 0.827 | 0.160 | 16 | 56956804 | regulatory region variant | C/A | snv | 0.29 | 20 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 20 | ||
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 19 | |
rs478442 | 0.851 | 0.120 | 2 | 21176344 | intergenic variant | G/C;T | snv | 18 | |||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 18 | ||
rs7703051 | 0.851 | 0.120 | 5 | 75329662 | intron variant | C/A | snv | 0.38 | 18 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 17 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 16 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 15 | |||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 14 | ||
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 13 |