Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
rs9825823 | 0.851 | 0.080 | 3 | 61096480 | intron variant | T/C | snv | 0.47 | 2 | ||
rs9364726 | 0.882 | 0.040 | 6 | 164236705 | intergenic variant | A/G | snv | 6.5E-02 | 3 | ||
rs9321987 | 0.925 | 0.040 | 6 | 144709148 | intron variant | C/T | snv | 0.40 | 3 | ||
rs853679 | 0.851 | 0.160 | 6 | 28329086 | intron variant | C/A | snv | 0.20 | 4 | ||
rs80278479 | 0.925 | 0.040 | 6 | 50758466 | intron variant | C/G | snv | 3.0E-03 | 3 | ||
rs7973260 | 0.851 | 0.120 | 12 | 117937681 | intron variant | A/G | snv | 0.83 | 2 | ||
rs7828021 | 0.925 | 0.040 | 8 | 49727454 | intergenic variant | C/G;T | snv | 3 | |||
rs782212 | 0.925 | 0.040 | 1 | 72479983 | intron variant | C/T | snv | 0.34 | 2 | ||
rs78087832 | 0.925 | 0.040 | 2 | 224600060 | intergenic variant | C/T | snv | 2.4E-03 | 3 | ||
rs77945277 | 0.925 | 0.040 | 14 | 34840969 | intron variant | A/G | snv | 4.9E-03 | 3 | ||
rs77826363 | 0.882 | 0.040 | 6 | 1128802 | intergenic variant | G/T | snv | 2.2E-02 | 3 | ||
rs76767803 | 0.925 | 0.040 | 3 | 36230378 | intergenic variant | C/T | snv | 0.16 | 2 | ||
rs760161369 | 0.882 | 0.040 | 1 | 11800214 | missense variant | G/A;C | snv | 2.8E-05; 4.0E-06 | 1 | ||
rs75995702 | 0.925 | 0.040 | 11 | 42785177 | intergenic variant | C/G;T | snv | 3 | |||
rs75921243 | 0.925 | 0.040 | 8 | 9988356 | intron variant | T/G | snv | 1.9E-02 | 2 | ||
rs7555693 | 0.925 | 0.040 | 1 | 106295917 | intergenic variant | G/A | snv | 0.45 | 3 | ||
rs74860738 | 0.925 | 0.040 | 11 | 80671683 | intergenic variant | G/A | snv | 7.2E-02 | 3 | ||
rs73425402 | 0.925 | 0.040 | 12 | 77503518 | intron variant | T/A | snv | 4.1E-02 | 3 | ||
rs7189979 | 0.925 | 0.040 | 16 | 12536330 | intron variant | A/C;G;T | snv | 3 | |||
rs6740584 | 0.882 | 0.040 | 2 | 207564627 | intron variant | T/C | snv | 0.37 | 1 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 4 | |
rs6586354 | 0.851 | 0.040 | 1 | 234897489 | intron variant | G/A | snv | 0.25 | 4 | ||
rs6546604 | 0.925 | 0.040 | 2 | 70415675 | intron variant | G/A;T | snv | 3 | |||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 |