Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35320474 | 1.000 | 0.080 | 22 | 24441941 | 3 prime UTR variant | -/T | delins | 2 | |||
rs2709370 | 0.851 | 0.120 | 2 | 207517878 | intron variant | A/C | snv | 0.17 | 4 | ||
rs1042606 | 1.000 | 0.080 | 10 | 110510917 | 3 prime UTR variant | A/C | snv | 0.64 | 1 | ||
rs1245560 | 1.000 | 0.080 | 10 | 72077662 | intron variant | A/C | snv | 0.51 | 1 | ||
rs1457319153 | 1.000 | 0.080 | 3 | 49531991 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
rs3786285 | 0.925 | 0.120 | 18 | 12008848 | intron variant | A/C;G | snv | 2 | |||
rs556493 | 1.000 | 0.080 | 6 | 147228161 | intron variant | A/C;G;T | snv | 1 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs2230912 | 0.752 | 0.280 | 12 | 121184393 | missense variant | A/G | snv | 0.13 | 0.12 | 16 | |
rs3093059 | 0.752 | 0.520 | 1 | 159715346 | upstream gene variant | A/G | snv | 0.13 | 11 | ||
rs956572 | 0.742 | 0.280 | 18 | 63153338 | intron variant | A/G | snv | 0.65 | 11 | ||
rs1390938 | 0.807 | 0.200 | 8 | 20179202 | missense variant | A/G | snv | 0.71 | 0.78 | 7 | |
rs187269 | 0.827 | 0.160 | 5 | 161329618 | 3 prime UTR variant | A/G | snv | 0.34 | 6 | ||
rs61749465 | 0.851 | 0.120 | 8 | 6414832 | missense variant | A/G | snv | 2.1E-03 | 1.9E-03 | 5 | |
rs6746896 | 0.851 | 0.120 | 2 | 96745212 | intergenic variant | A/G | snv | 0.26 | 4 | ||
rs6785 | 0.851 | 0.120 | 2 | 207603273 | 3 prime UTR variant | A/G | snv | 0.84 | 4 | ||
rs175174 | 0.882 | 0.120 | 22 | 20140031 | non coding transcript exon variant | A/G | snv | 0.44 | 3 | ||
rs1610037 | 0.925 | 0.120 | 18 | 910634 | 3 prime UTR variant | A/G | snv | 0.26 | 2 | ||
rs371131106 | 0.925 | 0.120 | 17 | 63485346 | missense variant | A/G | snv | 8.4E-05 | 1.6E-04 | 2 | |
rs3974590 | 0.925 | 0.120 | 18 | 11892846 | intron variant | A/G | snv | 0.35 | 2 | ||
rs613993 | 0.925 | 0.120 | 18 | 12028581 | non coding transcript exon variant | A/G | snv | 0.33 | 2 | ||
rs1010419 | 1.000 | 0.080 | 15 | 86992870 | intron variant | A/G | snv | 0.55 | 1 | ||
rs1049269 | 1.000 | 0.080 | 10 | 72060243 | 3 prime UTR variant | A/G | snv | 0.64 | 1 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 |