Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs112505971 10 27068541 intron variant A/C;G snv 13
rs3123543 1 212617344 intron variant T/A;C snv 13
rs3840870 17 50184820 3 prime UTR variant -/CTTG delins 13
rs76792961 16 243594 intron variant C/T snv 7.3E-03 13
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs9917425 20 16755400 intron variant G/T snv 0.16 13
rs7296503 12 41306962 intron variant C/T snv 0.57 13
rs4837892 9 121826025 intron variant G/T snv 0.36 13
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12