Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 10 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 8 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 7 | ||
rs5743618 | 0.677 | 0.360 | 4 | 38797027 | missense variant | C/A | snv | 0.53 | 0.51 | 6 | |
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs479844 | 0.851 | 0.160 | 11 | 65784486 | upstream gene variant | A/G | snv | 0.44 | 5 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 5 | |
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 5 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 4 | |
rs7512552 | 1.000 | 0.120 | 1 | 150293284 | upstream gene variant | T/C | snv | 0.63 | 4 | ||
rs9368699 | 0.851 | 0.200 | 6 | 31834764 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 4 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 4 | ||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 3 | ||
rs10791824 | 0.882 | 0.160 | 11 | 65791795 | intron variant | A/G;T | snv | 3 | |||
rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 3 | |||
rs1295686 | 0.882 | 0.160 | 5 | 132660151 | intron variant | T/A;C | snv | 0.68 | 3 | ||
rs12081541 | 0.925 | 0.160 | 1 | 152468890 | intergenic variant | T/C | snv | 8.9E-02 | 2 | ||
rs1384974 | 0.925 | 0.120 | 3 | 177009491 | downstream gene variant | T/C | snv | 9.6E-02 | 2 | ||
rs1528473 | 0.925 | 0.120 | 15 | 55094545 | downstream gene variant | A/G | snv | 7.6E-02 | 2 | ||
rs17728338 | 0.851 | 0.160 | 5 | 151098757 | downstream gene variant | G/A | snv | 7.1E-02 | 2 | ||
rs67766926 | 0.925 | 0.120 | 2 | 60936446 | downstream gene variant | C/G | snv | 0.17 | 2 | ||
rs7130588 | 0.882 | 0.200 | 11 | 76559639 | regulatory region variant | A/G | snv | 0.29 | 2 | ||
rs9302874 | 0.925 | 0.120 | 17 | 78284479 | intergenic variant | C/T | snv | 0.24 | 2 |