Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs4820268 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs9399137 0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs77542162 1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs738408 0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs5030868 0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04 9