Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 40 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs33939927 | 0.708 | 0.120 | 12 | 40310434 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 24 | ||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 13 | |||
rs7895833 | 0.742 | 0.440 | 10 | 67863299 | upstream gene variant | G/A;C | snv | 12 | |||
rs4717806 | 0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv | 9 | |||
rs2298813 | 0.790 | 0.120 | 11 | 121522975 | missense variant | G/A;T | snv | 7.2E-02; 4.0E-06 | 7 | ||
rs104894103 | 0.807 | 0.280 | 9 | 32974495 | stop gained | C/G;T | snv | 4.0E-06; 1.6E-04 | 6 | ||
rs7354779 | 0.827 | 0.200 | 21 | 44250887 | missense variant | T/C | snv | 0.21 | 6 | ||
rs12344615 | 0.851 | 0.080 | 9 | 83666280 | intron variant | A/C;G | snv | 4 | |||
rs59007384 | 0.851 | 0.080 | 19 | 44893408 | intron variant | G/A;T | snv | 4 | |||
rs5978930 | 0.882 | 0.080 | X | 8642266 | intron variant | T/C;G | snv | 4 | |||
rs9357347 | 0.851 | 0.080 | 6 | 41182853 | intergenic variant | A/C;T | snv | 4 | |||
rs1859788 | 0.925 | 0.080 | 7 | 100374211 | missense variant | A/C;G | snv | 4.0E-06; 0.65 | 3 | ||
rs1451603364 | 0.925 | 0.120 | 11 | 27658411 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs4837766 | 0.925 | 0.080 | 9 | 120402006 | intron variant | A/C;G;T | snv | 2 | |||
rs4978818 | 0.925 | 0.120 | 9 | 109509949 | intron variant | G/A;C;T | snv | 2 | |||
rs528528 | 0.925 | 0.080 | 7 | 103748638 | intron variant | T/A;C | snv | 2 | |||
rs63750048 | 0.925 | 0.080 | 1 | 226883817 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs1130399 | 1.000 | 0.040 | 6 | 32661978 | missense variant | G/A;T | snv | 0.20 | 1 | ||
rs1334496 | 1.000 | 0.040 | X | 137178554 | intergenic variant | C/A;T | snv | 1 | |||
rs227959 | 1.000 | 0.040 | 17 | 3406923 | upstream gene variant | C/T | snv | 1 |