Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs1555968941 | 0.752 | 0.280 | 12 | 2653847 | missense variant | G/A;C | snv | 31 | |||
rs886041091 | 0.807 | 0.120 | 9 | 84751990 | missense variant | A/G | snv | 18 | |||
rs387906799 | 0.742 | 0.200 | 2 | 240788118 | missense variant | G/A | snv | 17 | |||
rs1555817157 | 0.742 | 0.280 | 20 | 25339320 | frameshift variant | TCTTCCTCAGGCG/- | del | 16 | |||
rs672601370 | 0.790 | 0.160 | 2 | 240775863 | missense variant | G/A | snv | 13 | |||
rs672601369 | 0.790 | 0.120 | 2 | 240783780 | missense variant | C/T | snv | 10 | |||
rs886037832 | 0.851 | 0.280 | 10 | 100988541 | frameshift variant | T/- | delins | 9 | |||
rs730882246 | 0.807 | 0.200 | 14 | 74494329 | missense variant | G/A | snv | 8 | |||
rs672601367 | 0.851 | 0.080 | 2 | 240785066 | missense variant | T/G | snv | 7 | |||
rs672601363 | 0.851 | 0.080 | 2 | 240788109 | missense variant | C/T | snv | 6 | |||
rs672601366 | 0.851 | 0.120 | 2 | 240786339 | missense variant | C/G | snv | 6 | |||
rs1057517686 | 0.827 | 0.120 | 1 | 1529299 | missense variant | C/T | snv | 5 | |||
rs1555303073 | 0.851 | 0.120 | 13 | 110176912 | missense variant | C/T | snv | 5 | |||
rs1057518927 | 0.925 | 0.080 | 10 | 124402952 | missense variant | T/C | snv | 4 | |||
rs672601371 | 0.925 | 0.080 | 2 | 240783791 | missense variant | A/T | snv | 4 | |||
rs80356529 | 0.827 | 0.240 | 3 | 193643996 | missense variant | G/A;C | snv | 4 | |||
rs1057519286 | 0.882 | 0.080 | 1 | 29196234 | stop gained | A/C;G | snv | 3 | |||
rs1057519287 | 0.882 | 0.080 | 1 | 29216612 | frameshift variant | TGAT/- | delins | 3 | |||
rs119103265 | 0.827 | 0.120 | 1 | 12002033 | missense variant | C/T | snv | 3 | |||
rs730882240 | 1.000 | 0.080 | 16 | 574693 | stop gained | C/T | snv | 2.1E-05 | 3 | ||
rs387906930 | 0.790 | 0.360 | 4 | 6301846 | missense variant | C/G;T | snv | 2 | |||
rs74315205 | 0.807 | 0.360 | 4 | 6302385 | missense variant | G/A | snv | 2 | |||
rs80356524 | 0.882 | 0.200 | 19 | 45553777 | missense variant | C/T | snv | 2 | |||
rs1020764190 | 0.925 | 0.120 | 18 | 12351330 | missense variant | G/A | snv | 1 |