Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852671 | 0.790 | 0.160 | 11 | 17394295 | missense variant | C/T | snv | 10 | |||
rs3732581 | 0.790 | 0.120 | 3 | 183840614 | missense variant | C/G;T | snv | 0.46; 1.2E-05 | 9 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 12 | ||
rs2066808 | 0.807 | 0.280 | 12 | 56344189 | intron variant | A/G | snv | 0.21 | 8 | ||
rs628031 | 0.807 | 0.280 | 6 | 160139813 | missense variant | A/C;G | snv | 5.3E-05; 0.63 | 8 | ||
rs11171806 | 0.807 | 0.360 | 12 | 56339747 | synonymous variant | G/A | snv | 4.9E-02 | 4.5E-02 | 7 | |
rs683369 | 0.807 | 0.360 | 6 | 160130172 | missense variant | G/A;C;T | snv | 4.0E-06; 0.83; 4.0E-06 | 7 | ||
rs1033656351 | 0.827 | 0.160 | 12 | 121232997 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 7 | |
rs121909731 | 0.851 | 0.120 | 10 | 87057692 | missense variant | G/A;C | snv | 4.0E-06 | 7 | ||
rs2920502 | 0.851 | 0.160 | 3 | 12287696 | intron variant | G/C | snv | 0.27 | 6 | ||
rs146488435 | 0.851 | 0.080 | 17 | 63533914 | missense variant | C/G;T | snv | 8.0E-06; 6.4E-05 | 5 | ||
rs1057518775 | 0.851 | 0.160 | 11 | 17387907 | missense variant | G/A;C | snv | 4 | |||
rs1057515572 | 0.882 | 0.200 | 7 | 5987033 | frameshift variant | GC/ACT | delins | 8 | |||
rs121909730 | 0.882 | 0.040 | 10 | 87053380 | missense variant | G/A | snv | 4 | |||
rs9402571 | 0.882 | 0.080 | 6 | 134167822 | downstream gene variant | T/G | snv | 0.22 | 4 | ||
rs1003887 | 0.882 | 0.240 | 19 | 17816591 | 3 prime UTR variant | C/T | snv | 0.69 | 3 | ||
rs121913564 | 0.882 | 0.080 | 18 | 60371403 | missense variant | A/C | snv | 2.0E-05 | 1.4E-05 | 3 | |
rs2014355 | 0.925 | 0.120 | 12 | 120737721 | non coding transcript exon variant | T/C | snv | 0.22 | 4 | ||
rs79874540 | 0.925 | 0.080 | 2 | 231123707 | stop gained | G/A | snv | 1.5E-03 | 1.2E-03 | 4 | |
rs35568725 | 0.925 | 0.080 | 9 | 19119676 | missense variant | A/G | snv | 4.1E-02 | 4.0E-02 | 3 | |
rs146695489 | 0.925 | 0.160 | 11 | 17470170 | missense variant | T/C | snv | 2.5E-04 | 5.6E-05 | 2 | |
rs193922479 | 0.925 | 0.080 | 20 | 44424116 | missense variant | C/A;T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs225017 | 0.925 | 0.080 | 14 | 80200883 | 3 prime UTR variant | A/T | snv | 0.58 | 2 | ||
rs2288377 | 0.925 | 0.080 | 12 | 102480984 | intron variant | A/G;T | snv | 2 | |||
rs2918419 | 0.925 | 0.040 | 5 | 143342788 | intron variant | T/C | snv | 0.15 | 2 |