Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 5 | ||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 3 | ||
rs1517352 | 0.851 | 0.160 | 2 | 191066738 | intron variant | A/C | snv | 0.45 | 3 | ||
rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 2 | ||
rs4807569 | 0.925 | 0.120 | 19 | 1123379 | intron variant | A/C | snv | 0.25 | 2 | ||
rs9891119 | 0.882 | 0.120 | 17 | 42355962 | intron variant | A/C | snv | 0.36 | 2 | ||
rs12948909 | 0.925 | 0.120 | 17 | 42418584 | intron variant | A/C | snv | 0.24 | 1 | ||
rs16853571 | 1.000 | 0.040 | 4 | 41751113 | intron variant | A/C | snv | 9.9E-02 | 1 | ||
rs16931910 | 1.000 | 0.040 | 9 | 114856029 | intron variant | A/C | snv | 7.2E-02 | 1 | ||
rs17312836 | 1.000 | 0.040 | 16 | 50707551 | intron variant | A/C | snv | 0.33 | 1 | ||
rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 1 | ||
rs247660 | 1.000 | 0.040 | 5 | 85462322 | upstream gene variant | A/C | snv | 0.21 | 1 | ||
rs3135499 | 0.882 | 0.160 | 16 | 50732216 | splice donor variant | A/C | snv | 0.45 | 1 | ||
rs4855873 | 1.000 | 0.040 | 3 | 49421681 | non coding transcript exon variant | A/C | snv | 0.43 | 1 | ||
rs7186163 | 1.000 | 0.040 | 16 | 50652646 | downstream gene variant | A/C | snv | 0.63 | 1 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 2 | ||
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 2 | ||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 2 | ||
rs10512734 | 1.000 | 0.040 | 5 | 40393503 | intergenic variant | A/C;G | snv | 0.29 | 1 | ||
rs11871801 | 1.000 | 0.040 | 17 | 42418754 | intron variant | A/C;G | snv | 1 | |||
rs2302759 | 1.000 | 0.040 | 16 | 50793690 | intron variant | A/C;G | snv | 4.0E-06; 0.79 | 1 | ||
rs394522 | 1.000 | 0.040 | 6 | 166984583 | intron variant | A/C;G | snv | 1 | |||
rs7076156 | 0.925 | 0.120 | 10 | 62655424 | missense variant | A/C;G | snv | 0.80 | 1 | ||
rs740495 | 1.000 | 0.040 | 19 | 1124836 | intron variant | A/C;G | snv | 1 |