Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs104893689 0.790 0.200 3 122261589 missense variant G/A;C snv 10
rs121909262 0.851 0.120 3 122254304 missense variant C/G;T snv 5
rs193922442 0.827 0.120 3 122261589 frameshift variant G/- del 5
rs28936684 0.827 0.160 3 122261715 missense variant G/A;T snv 4.0E-06 5
rs104893705 0.882 0.120 3 122283896 stop gained C/A;G;T snv 4.0E-06 3
rs121909259 0.882 0.160 3 122261924 missense variant G/A snv 3
rs201858689 0.882 0.120 3 122284257 missense variant G/T snv 2.8E-05 3
rs104893690 0.925 0.120 3 122283699 missense variant G/A;T snv 2
rs104893700 1.000 0.080 3 122283963 missense variant G/A snv 1
rs104893707 1.000 0.080 3 122261588 stop gained C/A;T snv 1.6E-05 1
rs104893709 1.000 0.080 3 122257175 stop gained G/T snv 1
rs1060502861 1.000 0.080 3 122282156 missense variant G/A snv 1
rs869320729 1.000 0.080 3 122284195 frameshift variant CC/T delins 1