Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs201921722 | 0.925 | 0.040 | 11 | 123679999 | downstream gene variant | -/A | delins | 9.2E-06 | 3 | ||
rs34177316 | 0.925 | 0.040 | 4 | 40985283 | intron variant | A/-;AA;AAA | delins | 3 | |||
rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 1 | |
rs4810896 | 0.925 | 0.040 | 20 | 48918761 | upstream gene variant | A/C;G | snv | 2 | |||
rs7189979 | 0.925 | 0.040 | 16 | 12536330 | intron variant | A/C;G;T | snv | 3 | |||
rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 1 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 25 | |
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
rs17158930 | 0.851 | 0.040 | 7 | 111871082 | intron variant | A/G | snv | 0.25 | 4 | ||
rs12555870 | 0.925 | 0.040 | 9 | 23347726 | intron variant | A/G | snv | 0.36 | 3 | ||
rs1411216 | 0.925 | 0.040 | 9 | 24520196 | intergenic variant | A/G | snv | 0.73 | 3 | ||
rs143405544 | 0.925 | 0.040 | 5 | 65459777 | intron variant | A/G | snv | 4.8E-03 | 3 | ||
rs182377406 | 0.925 | 0.040 | 11 | 67449378 | upstream gene variant | A/G | snv | 4.5E-04 | 3 | ||
rs77945277 | 0.925 | 0.040 | 14 | 34840969 | intron variant | A/G | snv | 4.9E-03 | 3 | ||
rs9364726 | 0.882 | 0.040 | 6 | 164236705 | intergenic variant | A/G | snv | 6.5E-02 | 3 | ||
rs10233018 | 0.925 | 0.040 | 7 | 117883655 | non coding transcript exon variant | A/G | snv | 0.53 | 2 | ||
rs2221540 | 0.925 | 0.040 | 11 | 132846474 | intron variant | A/G | snv | 0.11 | 2 | ||
rs7973260 | 0.851 | 0.120 | 12 | 117937681 | intron variant | A/G | snv | 0.83 | 2 | ||
rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
rs319924 | 0.925 | 0.040 | 6 | 63777354 | intron variant | A/G;T | snv | 2 | |||
rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 1 | |||
rs16875288 | 0.851 | 0.040 | 5 | 5297087 | intron variant | A/T | snv | 0.22 | 4 |