Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs889312 | 0.732 | 0.360 | 5 | 56736057 | regulatory region variant | C/A | snv | 0.69 | 13 | ||
rs36115365 | 0.807 | 0.160 | 5 | 1313127 | upstream gene variant | G/A;C;T | snv | 6 | |||
rs7675998 | 0.827 | 0.360 | 4 | 163086668 | intergenic variant | A/G;T | snv | 4 | |||
rs9564966 | 0.851 | 0.120 | 13 | 73322084 | intergenic variant | A/G | snv | 0.52 | 4 | ||
rs12029406 | 0.882 | 0.120 | 1 | 199936700 | intergenic variant | C/T | snv | 0.36 | 3 | ||
rs9502893 | 0.827 | 0.120 | 6 | 1339954 | intergenic variant | C/G;T | snv | 3 | |||
rs10887710 | 0.925 | 0.120 | 10 | 80270029 | downstream gene variant | T/C | snv | 0.19 | 2 | ||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 2 | ||
rs1517037 | 0.882 | 0.120 | 18 | 59211042 | intergenic variant | C/T | snv | 0.23 | 2 | ||
rs1552462 | 0.925 | 0.120 | 11 | 7235910 | upstream gene variant | C/T | snv | 2.7E-02 | 2 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 2 | ||
rs6001516 | 0.925 | 0.120 | 22 | 39248198 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs10919791 | 0.925 | 0.240 | 1 | 199996040 | intergenic variant | G/A | snv | 0.22 | 1 | ||
rs2816938 | 1.000 | 0.120 | 1 | 200016240 | upstream gene variant | T/A | snv | 0.37 | 1 | ||
rs9363918 | 0.882 | 0.200 | 6 | 68432116 | intron variant | T/G | snv | 0.38 | 1 | ||
rs199976573 | 0.925 | 0.120 | 4 | 88132618 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 4 | |
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 20 | |||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 60 | ||
rs150495372 | 0.925 | 0.120 | 4 | 99313834 | missense variant | C/T | snv | 3.7E-04 | 3 | ||
rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
rs1693482 | 0.807 | 0.240 | 4 | 99342808 | missense variant | C/T | snv | 0.34 | 0.31 | 12 | |
rs35385902 | 0.807 | 0.240 | 4 | 99347122 | missense variant | C/A;T | snv | 2.0E-05; 1.1E-03 | 9 | ||
rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
rs4994 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 65 | |
rs1209809979 | 0.925 | 0.120 | 1 | 45568989 | missense variant | A/G | snv | 4.0E-06 | 3 |