Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11613352 | 0.827 | 0.160 | 12 | 57398797 | intron variant | C/T | snv | 0.19 | 5 | ||
rs11681351 | 0.925 | 0.120 | 2 | 27520556 | intron variant | G/A | snv | 0.36 | 3 | ||
rs11974409 | 0.925 | 0.120 | 7 | 73575060 | intron variant | A/G | snv | 0.16 | 6 | ||
rs12056034 | 0.882 | 0.160 | 7 | 73464315 | intron variant | A/G | snv | 9.2E-02 | 4 | ||
rs13022873 | 0.882 | 0.120 | 2 | 27592643 | intron variant | A/C;T | snv | 6 | |||
rs13030345 | 0.925 | 0.120 | 2 | 27780307 | intron variant | G/T | snv | 0.15 | 3 | ||
rs17145713 | 0.925 | 0.120 | 7 | 73490480 | intron variant | C/T | snv | 0.21 | 6 | ||
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 7 | |||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs2293572 | 0.925 | 0.120 | 2 | 27505910 | intron variant | C/G | snv | 0.39 | 3 | ||
rs714052 | 0.925 | 0.120 | 7 | 73450539 | intron variant | A/G | snv | 9.2E-02 | 4 | ||
rs7586601 | 0.925 | 0.120 | 2 | 27361799 | intron variant | A/G | snv | 0.54 | 3 | ||
rs780092 | 0.827 | 0.160 | 2 | 27520287 | intron variant | A/G | snv | 0.18 | 5 | ||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs7800944 | 0.882 | 0.160 | 7 | 73621527 | intron variant | T/C | snv | 0.28 | 4 | ||
rs813592 | 0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 | 3 | |
rs814295 | 0.925 | 0.120 | 2 | 27520348 | intron variant | A/G | snv | 0.18 | 5 | ||
rs799166 | 0.925 | 0.120 | 7 | 73637602 | intergenic variant | C/G | snv | 0.16 | 4 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs1919127 | 0.925 | 0.120 | 2 | 27578626 | missense variant | T/C | snv | 0.31 | 0.27 | 6 | |
rs1919128 | 0.882 | 0.120 | 2 | 27578892 | missense variant | A/G | snv | 0.30 | 0.24 | 6 | |
rs3749147 | 0.882 | 0.120 | 2 | 27629051 | missense variant | G/A | snv | 0.23 | 0.20 | 6 | |
rs1528533 | 0.925 | 0.120 | 2 | 27372889 | non coding transcript exon variant | G/C | snv | 0.47 | 3 | ||
rs2074755 | 0.807 | 0.240 | 7 | 73462836 | non coding transcript exon variant | T/C | snv | 9.2E-02 | 4 |