Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 34 | |
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 27 | ||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs3918226 | 0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 | 12 | ||
rs516246 | 0.925 | 0.160 | 19 | 48702915 | intron variant | C/T | snv | 0.38 | 0.45 | 10 | |
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 9 | ||
rs45446698 | 0.807 | 0.120 | 7 | 99735325 | upstream gene variant | T/G | snv | 2.7E-02 | 9 | ||
rs17367504 | 1.000 | 0.040 | 1 | 11802721 | intron variant | A/G | snv | 0.14 | 9 | ||
rs10814916 | 0.851 | 0.200 | 9 | 4293150 | intron variant | A/C | snv | 0.57 | 7 | ||
rs1042725 | 0.882 | 0.080 | 12 | 65964567 | 3 prime UTR variant | C/T | snv | 0.48 | 7 | ||
rs8756 | 0.882 | 0.200 | 12 | 65965972 | 3 prime UTR variant | C/A | snv | 0.56 | 7 | ||
rs900400 | 0.925 | 0.080 | 3 | 157080986 | upstream gene variant | T/C | snv | 0.36 | 7 | ||
rs9366778 | 0.925 | 0.120 | 6 | 31301396 | intron variant | G/A | snv | 0.47 | 7 | ||
rs2168101 | 0.827 | 0.200 | 11 | 8233861 | intron variant | C/A | snv | 0.24 | 7 | ||
rs3740360 | 0.827 | 0.240 | 10 | 94265734 | intron variant | A/C | snv | 9.7E-02 | 8.4E-02 | 7 | |
rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 7 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 6 | |||||
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
rs2274224 | 0.882 | 0.080 | 10 | 94279840 | missense variant | G/A;C | snv | 8.8E-05; 0.44 | 6 | ||
rs9379084 | 0.882 | 0.160 | 6 | 7231610 | missense variant | G/A | snv | 0.11 | 8.9E-02 | 6 | |
rs72681869 | 14 | 50188639 | missense variant | G/A;C | snv | 4.0E-06; 4.1E-03 | 6 | ||||
rs10173538 | 2 | 159712765 | intron variant | C/G;T | snv | 5 |