Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs57942103 1.000 0.040 8 105501233 intron variant A/C snv 0.25 3
rs11774829 8 104966140 intron variant T/A snv 7.6E-02 3
rs35783704 8 104954030 intron variant G/A snv 7.2E-02 2
rs4734879 8 105570896 intron variant A/G snv 0.31 2
rs10093110 1.000 0.040 8 105553186 intron variant G/A;T snv 1
rs28416651 1.000 0.040 8 105552424 intron variant G/A;C snv 1
rs7819593 8 105102944 intron variant T/C snv 0.35 1
rs284489 0.882 0.080 8 104945792 intron variant A/G snv 0.45 1
rs1350723 8 105218944 intron variant G/A snv 0.69 1
rs1460583 1.000 0.040 8 105096365 intron variant T/C snv 0.26 1
rs16872085 8 104945312 intron variant A/G snv 7.6E-02 1
rs284491 0.925 0.040 8 104946405 intron variant C/T snv 0.45 1
rs12678719 1.000 8 105503826 intron variant C/G snv 0.37 1
rs7837523 8 105517074 intron variant A/T snv 0.80 1
rs1375961 8 105535755 intron variant T/G snv 0.14 1
rs12546444 1.000 0.080 8 105346392 intron variant A/T snv 8.0E-02 1
rs17210179 8 105333241 intron variant C/T snv 0.11 1
rs1383592 8 105418448 intron variant G/A snv 0.26 1
rs2342781 1.000 0.040 8 105253492 intron variant C/G;T snv 1
rs72679151 8 104614889 intron variant C/T snv 0.17 1
rs7832219 8 105566749 intron variant T/C snv 0.31 1
rs3832566 8 105561297 intron variant A/- delins 0.29 1
rs2343592 8 105560042 intron variant A/G snv 0.30 1