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 | 14 | ||
rs36115365 | 0.807 | 0.160 | 5 | 1313127 | upstream gene variant | G/A;C;T | snv | 7 | |||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 5 | ||
rs7675998 | 0.827 | 0.360 | 4 | 163086668 | intergenic variant | A/G;T | snv | 5 | |||
rs9502893 | 0.827 | 0.120 | 6 | 1339954 | intergenic variant | C/G;T | snv | 5 | |||
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 | ||
rs1517037 | 0.882 | 0.120 | 18 | 59211042 | intergenic variant | C/T | snv | 0.23 | 3 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 3 | ||
rs9363918 | 0.882 | 0.200 | 6 | 68432116 | intron variant | T/G | snv | 0.38 | 3 | ||
rs9543325 | 0.882 | 0.200 | 13 | 73342491 | regulatory region variant | C/G;T | snv | 3 | |||
rs10887710 | 0.925 | 0.120 | 10 | 80270029 | downstream gene variant | T/C | snv | 0.19 | 2 | ||
rs10919791 | 0.925 | 0.240 | 1 | 199996040 | intergenic variant | G/A | snv | 0.22 | 2 | ||
rs1552462 | 0.925 | 0.120 | 11 | 7235910 | upstream gene variant | C/T | snv | 2.7E-02 | 2 | ||
rs2816938 | 1.000 | 0.120 | 1 | 200016240 | upstream gene variant | T/A | snv | 0.37 | 2 | ||
rs6001516 | 0.925 | 0.120 | 22 | 39248198 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs9573163 | 0.925 | 0.120 | 13 | 73334709 | regulatory region variant | C/G;T | snv | 2 | |||
rs12478462 | 1.000 | 0.120 | 2 | 152798206 | intergenic variant | T/G | snv | 0.28 | 1 | ||
rs1486134 | 1.000 | 0.120 | 2 | 67412637 | downstream gene variant | G/C;T | snv | 1 | |||
rs17275283 | 1.000 | 0.120 | 11 | 96970814 | intron variant | T/C | snv | 0.26 | 1 | ||
rs1944788 | 1.000 | 0.120 | 11 | 96947703 | intron variant | T/C | snv | 0.27 | 1 | ||
rs2218400 | 1.000 | 0.120 | 13 | 63564941 | intergenic variant | C/A | snv | 0.34 | 1 | ||
rs6537481 | 1.000 | 0.120 | 4 | 147474942 | intergenic variant | A/C;G | snv | 1 | |||
rs7330800 | 1.000 | 0.120 | 13 | 63573938 | intergenic variant | A/C;T | snv | 1 | |||
rs199976573 | 0.925 | 0.120 | 4 | 88132618 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 4 |