Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1056198 | 0.925 | 0.040 | 20 | 49939692 | intron variant | C/T | snv | 0.34 | 2 | ||
rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs11652075 | 0.882 | 0.040 | 17 | 80205094 | missense variant | C/T | snv | 0.41 | 0.40 | 1 | |
rs12445568 | 0.925 | 0.040 | 16 | 30993491 | splice region variant | T/C | snv | 0.39 | 0.38 | 2 | |
rs12489120 | 1.000 | 0.040 | 3 | 4978778 | intron variant | C/A;G;T | snv | 1 | |||
rs1250544 | 0.882 | 0.080 | 10 | 79273128 | intron variant | G/A | snv | 0.32 | 3 | ||
rs12884468 | 0.925 | 0.040 | 14 | 35383280 | downstream gene variant | T/C | snv | 0.47 | 2 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 4 | ||
rs17716942 | 0.925 | 0.040 | 2 | 162404181 | intron variant | T/C | snv | 9.6E-02 | 2 | ||
rs17728338 | 0.851 | 0.160 | 5 | 151098757 | downstream gene variant | G/A | snv | 7.1E-02 | 2 | ||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 2 | |
rs181359 | 0.882 | 0.080 | 22 | 21574352 | intron variant | G/A | snv | 0.21 | 2 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 4 | |
rs2066819 | 0.925 | 0.040 | 12 | 56356420 | intron variant | C/T | snv | 4.9E-02 | 4.5E-02 | 2 | |
rs2233278 | 0.925 | 0.040 | 5 | 151087628 | 5 prime UTR variant | G/C;T | snv | 4.8E-02 | 2 | ||
rs2395029 | 0.790 | 0.320 | 6 | 31464003 | non coding transcript exon variant | T/G | snv | 2.7E-02 | 2.4E-02 | 7 | |
rs2675662 | 0.925 | 0.040 | 10 | 73839369 | intron variant | A/G | snv | 0.55 | 2 | ||
rs2675669 | 1.000 | 0.040 | 10 | 73894114 | intergenic variant | C/T | snv | 0.55 | 1 | ||
rs27432 | 0.925 | 0.040 | 5 | 96783569 | intron variant | A/C;G | snv | 2 | |||
rs27524 | 0.851 | 0.160 | 5 | 96766240 | intron variant | A/G | snv | 0.61 | 1 | ||
rs28998802 | 0.807 | 0.120 | 17 | 27797882 | intron variant | G/A | snv | 0.11 | 6 | ||
rs30187 | 0.732 | 0.360 | 5 | 96788627 | missense variant | T/A;C | snv | 0.62 | 1 | ||
rs3135388 | 0.807 | 0.240 | 6 | 32445274 | downstream gene variant | A/G | snv | 0.90 | 1 | ||
rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 3 | |
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 20 |