Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs174601 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2075290 0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs6589566 0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs676210 0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs11570255 1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs11571151 11 101127486 missense variant C/G;T snv 6
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs17240378 16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6