Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2420371 | 1 | 169522317 | intron variant | G/A | snv | 0.95 | 4 | ||||
rs1413885 | 1 | 65349976 | intron variant | C/T | snv | 0.72 | 2 | ||||
rs4133289 | 1 | 159484147 | downstream gene variant | C/T | snv | 0.16 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 8 | ||
rs13022873 | 0.882 | 0.120 | 2 | 27592643 | intron variant | A/C;T | snv | 6 | |||
rs1919127 | 0.925 | 0.120 | 2 | 27578626 | missense variant | T/C | snv | 0.31 | 0.27 | 6 | |
rs1919128 | 0.882 | 0.120 | 2 | 27578892 | missense variant | A/G | snv | 0.30 | 0.24 | 6 | |
rs2911711 | 0.925 | 0.120 | 2 | 27527679 | downstream gene variant | T/A | snv | 0.58 | 6 | ||
rs3749147 | 0.882 | 0.120 | 2 | 27629051 | missense variant | G/A | snv | 0.23 | 0.20 | 6 | |
rs4666002 | 0.925 | 0.120 | 2 | 27617773 | intron variant | G/A;C | snv | 6 | |||
rs10208529 | 0.925 | 0.120 | 2 | 27563321 | intron variant | A/T | snv | 0.28 | 5 | ||
rs12467476 | 0.925 | 0.120 | 2 | 27602848 | intron variant | T/C | snv | 0.23 | 5 | ||
rs12478841 | 0.925 | 0.120 | 2 | 27588855 | intron variant | A/G | snv | 0.27 | 5 | ||
rs13002853 | 0.925 | 0.120 | 2 | 27630378 | intron variant | C/G | snv | 0.20 | 5 | ||
rs2384656 | 0.925 | 0.120 | 2 | 27609188 | intron variant | A/G | snv | 0.27 | 5 | ||
rs4665382 | 0.925 | 0.120 | 2 | 27560934 | intron variant | T/C | snv | 0.23 | 5 | ||
rs4665383 | 0.925 | 0.120 | 2 | 27568688 | synonymous variant | C/G | snv | 0.24 | 5 | ||
rs4665987 | 0.925 | 0.120 | 2 | 27532958 | upstream gene variant | G/A;T | snv | 5 | |||
rs4665991 | 0.925 | 0.120 | 2 | 27543417 | intron variant | G/A | snv | 0.24 | 5 | ||
rs4666000 | 0.925 | 0.120 | 2 | 27616502 | intron variant | T/C | snv | 0.28 | 5 | ||
rs6760250 | 0.925 | 0.120 | 2 | 27589385 | intron variant | G/A;C | snv | 5 |