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 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs4820268 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8