Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 40 | ||
rs10106 | 0.851 | 0.200 | 9 | 127813796 | 3 prime UTR variant | T/C | snv | 0.45 | 4 | ||
rs1020608187 | 1.000 | 0.120 | 12 | 113398843 | missense variant | C/G | snv | 7.0E-06 | 1 | ||
rs10235796 | 0.882 | 0.120 | 7 | 50394939 | intron variant | T/C | snv | 0.82 | 3 | ||
rs10272724 | 0.882 | 0.200 | 7 | 50409515 | downstream gene variant | T/C | snv | 0.24 | 4 | ||
rs1039659576 | 0.689 | 0.520 | 1 | 236803473 | missense variant | A/G | snv | 21 | |||
rs10417924 | 1.000 | 0.120 | 19 | 41327262 | intron variant | T/C | snv | 0.86 | 1 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1043618 | 0.752 | 0.280 | 6 | 31815730 | 5 prime UTR variant | G/A;C;T | snv | 0.39; 2.0E-05; 4.0E-06 | 9 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs104893636 | 0.882 | 0.120 | 2 | 176151875 | missense variant | A/C;T | snv | 5.2E-06; 7.9E-04 | 3 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs1051296 | 0.882 | 0.120 | 21 | 45514947 | 3 prime UTR variant | A/C | snv | 0.43 | 0.44 | 3 | |
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs10519612 | 0.882 | 0.120 | 4 | 141732548 | intron variant | A/C | snv | 0.10 | 3 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1057519743 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 5 | |||
rs1057519866 | 0.851 | 0.120 | 10 | 103093198 | missense variant | C/T | snv | 5 | |||
rs1061581 | 0.827 | 0.200 | 6 | 31816809 | synonymous variant | G/A | snv | 5 | |||
rs10740055 | 0.790 | 0.240 | 10 | 61958720 | intron variant | C/A | snv | 0.49 | 7 | ||
rs1076991 | 0.925 | 0.200 | 14 | 64388323 | 5 prime UTR variant | T/C;G | snv | 0.45; 8.1E-06 | 2 | ||
rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 10 | ||
rs10821938 | 0.925 | 0.120 | 10 | 61965014 | intron variant | A/C | snv | 0.56 | 1 | ||
rs10828317 | 0.776 | 0.280 | 10 | 22550699 | missense variant | T/C | snv | 8 | |||
rs10994982 | 0.790 | 0.120 | 10 | 61950345 | intron variant | A/G | snv | 0.49 | 7 |