Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11655505 0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs1467465 0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1800709 0.851 0.160 17 43093010 missense variant G/A snv 1.7E-03 1.4E-03 6
rs1800751 0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 5
rs190900046 0.827 0.160 17 43104197 synonymous variant A/C snv 8.0E-06 4.2E-05 5
rs2363956 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
rs2665390 0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs273900729 0.925 0.160 17 43082529 missense variant A/G snv 2
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs3177427 0.827 0.160 14 77326864 stop gained G/A;C;T snv 5
rs372038369 0.882 0.160 17 35101233 missense variant G/A;T snv 1.2E-05 1.4E-05 3
rs41293521 0.925 0.160 13 32394724 missense variant T/C snv 2.9E-04 2.5E-04 2
rs4987046 0.925 0.160 13 32319134 missense variant A/G snv 1.6E-03 1.6E-03 4
rs56307747 0.776 0.160 7 74059952 missense variant G/A;C snv 4.0E-06 8
rs587780128 0.882 0.160 7 152649010 missense variant G/A snv 1.2E-05 3.5E-05 3
rs587782818 0.790 0.160 17 58703325 stop gained C/G snv 6.4E-05; 4.0E-06 1.4E-05 8
rs61755649 0.882 0.160 14 67885891 missense variant C/T snv 6.8E-05 4.9E-05 3
rs638820 0.827 0.160 1 109667284 intron variant G/A snv 0.52 5
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 5
rs748876625 0.807 0.160 17 43104122 missense variant C/A;G snv 1.2E-05 10
rs750042441 0.827 0.160 11 101128367 missense variant G/A;C snv 6.1E-05; 4.3E-06 5
rs764918809 0.827 0.160 12 68839337 missense variant T/C snv 4.0E-06 6
rs786203319 0.827 0.160 17 43115759 missense variant G/A snv 6
rs80356897 0.827 0.160 17 43099853 missense variant A/G snv 5
rs80359078 0.882 0.160 13 32370430 missense variant G/A snv 3.2E-05 2.1E-05 3