Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397517108 | 0.790 | 0.120 | 7 | 55181312 | missense variant | GC/TT | mnv | 9 | |||
rs754332870 | 0.790 | 0.240 | 17 | 7676240 | missense variant | C/G | snv | 4.0E-06 | 9 | ||
rs4645978 | 0.827 | 0.120 | 1 | 15525539 | intron variant | C/A;T | snv | 8 | |||
rs10810657 | 0.827 | 0.080 | 9 | 16884588 | regulatory region variant | T/A;G | snv | 7 | |||
rs59912467 | 0.790 | 0.120 | 19 | 1223126 | missense variant | C/G;T | snv | 5.2E-03; 4.1E-06 | 7 | ||
rs1057520018 | 0.807 | 0.080 | 19 | 1223124 | missense variant | T/C | snv | 6 | |||
rs12108497 | 0.851 | 0.080 | 4 | 184650403 | intron variant | C/G;T | snv | 6 | |||
rs1389500636 | 0.827 | 0.080 | 7 | 55156796 | missense variant | G/A | snv | 6 | |||
rs1454328441 | 0.827 | 0.200 | 1 | 155192002 | missense variant | G/A;T | snv | 4.6E-06; 9.1E-06 | 6 | ||
rs35407 | 0.807 | 0.080 | 5 | 33946466 | 3 prime UTR variant | A/C;G | snv | 6 | |||
rs5491 | 0.827 | 0.160 | 19 | 10274864 | missense variant | A/G;T | snv | 4.0E-06; 2.8E-02 | 6 | ||
rs7208422 | 0.807 | 0.120 | 17 | 78134494 | missense variant | A/C;T | snv | 4.0E-06; 0.51 | 6 | ||
rs2273953 | 0.851 | 0.120 | 1 | 3682336 | 5 prime UTR variant | G/A;T | snv | 0.20; 3.3E-04 | 5 | ||
rs2299939 | 0.827 | 0.080 | 10 | 87897393 | intron variant | C/A;T | snv | 5 | |||
rs587783064 | 0.851 | 0.120 | 17 | 7669626 | missense variant | C/A;T | snv | 5 | |||
rs1057520039 | 0.882 | 0.200 | 19 | 1207169 | stop gained | C/G;T | snv | 4 | |||
rs58330629 | 0.851 | 0.120 | 17 | 41586461 | missense variant | C/A;G;T | snv | 4 | |||
rs765660823 | 0.882 | 0.200 | 1 | 162778720 | missense variant | A/C | snv | 1.9E-04 | 4 | ||
rs868438023 | 0.882 | 0.080 | 15 | 40382906 | missense variant | C/T | snv | 4 | |||
rs1770474 | 0.925 | 0.080 | 10 | 91833770 | intron variant | G/A;T | snv | 3 | |||
rs267598140 | 0.925 | 0.080 | 1 | 162778600 | missense variant | T/A;G | snv | 3 | |||
rs471692 | 0.925 | 0.080 | 17 | 40400518 | intron variant | T/A;C | snv | 0.79 | 3 | ||
rs74664507 | 1.000 | 0.040 | 9 | 16913838 | upstream gene variant | T/A | snv | 3 | |||
rs804270 | 0.882 | 0.080 | 8 | 11770112 | 5 prime UTR variant | G/C;T | snv | 3 | |||
rs121913082 | 1.000 | 0.040 | 10 | 89014205 | missense variant | A/G | snv | 2 |