Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 78 | ||
rs121912651 | 0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 | 53 | ||
rs397517132 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 48 | |||
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 42 | ||
rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
rs121912654 | 0.683 | 0.400 | 17 | 7675143 | missense variant | C/A;T | snv | 4.0E-05 | 21 | ||
rs750893877 | 0.807 | 0.320 | 17 | 7674258 | synonymous variant | G/A | snv | 8.0E-06 | 7 | ||
rs751306825 | 0.925 | 0.080 | 2 | 29220759 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs73070954 | 0.925 | 0.040 | 2 | 208248572 | missense variant | C/T | snv | 3.5E-03 | 1.4E-02 | 2 | |
rs749395621 | 0.925 | 0.040 | 15 | 90087536 | missense variant | T/C;G | snv | 4.0E-06; 3.6E-05 | 2 | ||
rs1244270149 | 1.000 | 0.040 | 2 | 29220746 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs1330260382 | 1.000 | 0.040 | 4 | 1801390 | missense variant | G/A | snv | 6.5E-06 | 1 | ||
rs1555525857 | 1.000 | 0.040 | 17 | 7674935 | missense variant | C/A;T | snv | 1 |