Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2076349 0.882 0.120 1 209626885 missense variant C/T snv 0.13 0.13 3
rs2491132 0.925 0.240 1 30876800 missense variant C/A;G;T snv 8.3E-06; 0.15 3
rs2605100 1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs45487298 0.882 0.120 1 209706871 intron variant -/A delins 3
rs726344 0.882 0.120 1 32867503 intron variant G/A snv 0.16 3
rs8179183 1.000 0.080 1 65610269 missense variant G/C;T snv 3
rs1040070 1.000 0.080 1 74512186 intron variant G/A;C snv 2
rs11208659 1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 2
rs12124383 1.000 0.080 1 155946002 downstream gene variant G/A snv 3.7E-03 2
rs12133337 0.925 0.160 1 167483453 intron variant T/C snv 0.17 2
rs1473 0.925 0.120 1 30940072 intron variant G/A snv 6.8E-02 2
rs1514174 1.000 0.080 1 74527379 intron variant C/T snv 0.44 2
rs1514177 1.000 0.080 1 74525718 intron variant C/G snv 0.49 2
rs17277372 0.925 0.120 1 172218334 intron variant A/G snv 0.22 2
rs201844852 0.925 0.080 1 157135581 missense variant C/G snv 4.8E-05 4.2E-05 2
rs35439639 1.000 0.080 1 206109537 3 prime UTR variant C/G;T snv 2
rs35608965 1.000 0.080 1 206116919 5 prime UTR variant A/G snv 4.9E-02 6.2E-02 2
rs3753519 0.925 0.200 1 209702170 intron variant T/A;C snv 2
rs3813627 1.000 0.080 1 161225358 upstream gene variant G/T snv 0.28 2
rs6429082 1.000 0.080 1 235436814 intron variant T/C snv 0.55 2
rs74315349 1.000 0.080 1 26913841 stop gained G/A;C snv 9.1E-05; 1.8E-04 2
rs7538490 0.925 0.120 1 162121540 intron variant T/C snv 0.70 2
rs757574299 1.000 0.080 1 65570511 missense variant C/G snv 1.6E-05 1.4E-05 2
rs10082248 1.000 0.080 1 209693771 intron variant A/G;T snv 1
rs10475 1.000 0.080 1 212620271 3 prime UTR variant T/C snv 0.76 1