Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs440446 0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs769452 0.925 0.160 19 44907853 missense variant T/C snv 2.5E-03 1.9E-03 2
rs769455 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs199768005 0.882 0.160 19 44909057 missense variant T/A snv 4.5E-04 4.9E-04 4
rs267606661 0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs140808909 0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs190853081 0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs533904656 1.000 0.080 19 44907768 missense variant G/A;C snv 1.8E-04; 8.2E-06 1
rs267606664 0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 5
rs201672011 1.000 0.080 19 44907807 missense variant G/A snv 1.2E-04 4.8E-04 2
rs28931579 19 44909236 missense variant A/C snv 9.5E-05 6.3E-05 1
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs759721023 1.000 0.080 19 44908936 missense variant G/A snv 8.4E-05 6.3E-05 1
rs121918395 19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05 1
rs121918392 0.925 0.040 19 44907777 missense variant G/A snv 3.6E-05 7.0E-06 2
rs28931578 19 44908751 missense variant G/A;C;T snv 3.2E-05 1
rs752600356 0.851 0.280 19 44908681 missense variant G/A;C snv 2.3E-05 1.4E-05 4
rs11542035 19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs121918396 1.000 0.080 19 44908979 stop gained G/A snv 1.6E-05 3.5E-05 1
rs761592007 0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs779569800 1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 1
rs11542029 1.000 0.080 19 44907864 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 1
rs28931576 19 44907894 missense variant A/G snv 1.2E-05 1.4E-05 1