Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137853222 0.925 0.160 17 63918072 missense variant C/A;G snv 2
rs137853223 0.851 0.160 17 63917337 missense variant C/T snv 7.0E-06 4
rs141842220 1.000 0.120 20 5119600 missense variant C/T snv 1
rs1448843898 1.000 0.120 4 1805608 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs145730800 1.000 0.120 16 89283963 missense variant G/A snv 5.2E-05 1.4E-04 1
rs1481733213
ATR
0.851 0.240 3 142568059 splice region variant T/C snv 5
rs151241066 1.000 0.120 1 220143003 missense variant G/A snv 2.0E-05 3.5E-05 1
rs1553761113
ATR
0.851 0.240 3 142507967 missense variant C/A snv 5
rs1555545033 0.807 0.160 17 40088306 missense variant C/T snv 7
rs1566902569 0.882 0.160 15 48460299 missense variant C/A snv 9
rs17881656 0.925 0.240 4 1804404 missense variant T/A;C snv 8.0E-06; 3.3E-03 3
rs180177456 0.925 0.160 1 247424426 missense variant G/A snv 2
rs201151136 1.000 0.120 8 19458486 missense variant T/C snv 1.4E-04 1.2E-04 1
rs2076738
TG
0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 6
rs2076739
TG
0.827 0.200 8 132971804 missense variant T/A snv 5
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs28931614 0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs28933068 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs33958176 1.000 0.120 15 98911384 missense variant G/A snv 1.6E-03 1.7E-03 1
rs372703574 0.851 0.160 20 38146858 missense variant G/A snv 4.8E-05 6.3E-05 4
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs387906623 0.882 0.120 15 48460258 missense variant C/T snv 4
rs387906918 0.925 0.120 16 88804027 missense variant G/A snv 7.0E-06 2
rs397514461 0.827 0.200 Y 640842 missense variant G/C snv 5
rs397514487 0.882 0.200 3 52149850 stop gained G/A snv 7.0E-06 3