Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs821633 0.882 0.160 1 232013187 intron variant T/C snv 0.37 3
rs946903 0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs10462020 0.925 0.160 1 7820623 missense variant T/G snv 0.17 0.16 2
rs10489744 0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs150404479 1.000 0.040 1 43222879 missense variant T/C snv 9.1E-03 9.8E-03 2
rs16836940 0.925 0.040 1 150444437 intron variant A/G snv 0.31 2
rs17018311 1.000 0.040 1 211981666 intron variant T/C snv 2.7E-02 2
rs707467 0.925 0.120 1 7801624 intron variant A/C snv 0.22 2
rs10489167 1.000 0.040 1 40710794 intron variant G/A snv 0.13 1
rs10889182 1.000 0.040 1 60532523 intron variant T/G snv 0.33 1
rs10889187 1.000 0.040 1 60545086 intron variant G/A snv 0.33 1
rs10889189 1.000 0.040 1 60559354 intron variant C/G snv 0.47 1
rs11207633 1.000 0.040 1 60541510 non coding transcript exon variant A/G snv 0.32 1
rs1125777 1.000 0.040 1 61366218 intron variant C/T snv 0.42 1
rs11805078 1.000 0.040 1 116381693 intron variant C/T snv 8.8E-02 1
rs12144699 1.000 0.040 1 59139525 intron variant G/A snv 2.3E-02 1
rs12563333 1.000 0.040 1 220484892 downstream gene variant C/T snv 3.7E-02 1
rs12568010 1.000 0.040 1 61366266 intron variant A/G snv 9.8E-02 1
rs16841582 1.000 0.040 1 231837888 intron variant C/G;T snv 1
rs17121983 1.000 0.040 1 61354400 intron variant C/G;T snv 1
rs17785382 1.000 0.040 1 53242281 intron variant A/G snv 0.31 1
rs186197500 1.000 0.040 1 178131084 intron variant C/A snv 8.8E-03 1
rs1927252 1.000 0.040 1 198264777 intron variant C/A snv 0.33 1
rs2070704 1.000 0.040 1 160142348 3 prime UTR variant A/G snv 0.22 1