Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 19 | ||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
rs12566888 | 0.807 | 0.280 | 1 | 156899255 | intron variant | G/T | snv | 0.26 | 7 | ||
rs5050 | 0.827 | 0.200 | 1 | 230714140 | intron variant | T/C;G | snv | 7 | |||
rs1861493 | 0.851 | 0.280 | 12 | 68157416 | intron variant | G/A | snv | 0.76 | 4 | ||
rs79524815 | 0.851 | 0.240 | 7 | 18658708 | intron variant | T/G | snv | 3.8E-02 | 4 | ||
rs16921209 | 0.882 | 0.160 | 10 | 20879174 | intron variant | C/G | snv | 4.6E-02 | 3 | ||
rs28834970 | 0.882 | 0.120 | 8 | 27337604 | intron variant | T/C | snv | 0.32 | 3 | ||
rs7637803 | 0.882 | 0.160 | 3 | 151371438 | intron variant | C/G;T | snv | 3 | |||
rs7849782 | 0.925 | 0.160 | 9 | 101664982 | intron variant | C/A;G;T | snv | 3 | |||
rs7572475 | 0.925 | 0.160 | 2 | 24670190 | intron variant | A/T | snv | 0.19 | 2 | ||
rs7922552 | 0.925 | 0.160 | 10 | 20896095 | intron variant | C/G;T | snv | 2 | |||
rs34487851 | 0.882 | 0.200 | 2 | 106026098 | regulatory region variant | A/G | snv | 0.28 | 3 | ||
rs730882070 | 1.000 | 0.040 | 18 | 75286265 | stop gained | G/A | snv | 1 | |||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs121918075 | 0.752 | 0.280 | 18 | 31598632 | missense variant | A/G | snv | 15 | |||
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs1035071612 | 0.763 | 0.240 | 19 | 11113361 | missense variant | C/A;T | snv | 4.0E-06 | 9 | ||
rs28939068 | 0.790 | 0.200 | 20 | 23635330 | missense variant | A/T | snv | 9 | |||
rs1394871591 | 0.827 | 0.200 | 9 | 104903619 | missense variant | G/C | snv | 4.8E-06 | 5 | ||
rs1297968881 | 0.882 | 0.200 | 21 | 26112137 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
rs63750973 | 0.882 | 0.120 | 21 | 25891792 | missense variant | G/A | snv | 3 | |||
rs2229634 | 0.851 | 0.240 | 6 | 33670403 | synonymous variant | C/A;T | snv | 4.0E-06; 0.33 | 4 |