Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11655081 0.851 0.080 17 68386068 intron variant T/C snv 0.18 7
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs374052333 0.763 0.320 3 132671032 stop gained C/G;T snv 4.0E-06 27
rs139455627 0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs74315442 0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs546151500 0.925 0.080 2 218643341 stop gained G/A;T snv 8.0E-06; 4.0E-06 5
rs1553547838 0.925 0.280 2 199328709 stop gained G/A snv 4
rs531630376 1.000 0.080 5 141955844 stop gained C/A snv 4.0E-06 4
rs1057519279 1.000 19 35720980 stop gained C/T snv 3
rs1057519281 1.000 19 35721775 stop gained C/T snv 3
rs121917762
TH
0.925 0.040 11 2165727 stop gained G/A;T snv 4.0E-06; 4.0E-06 3
rs137852968 0.925 0.080 20 3916955 stop gained C/A;T snv 4.0E-06; 1.2E-05; 3.6E-05 3
rs771610752
TH
0.925 0.040 11 2168614 stop gained G/A snv 6.2E-05 2.1E-05 3
rs121917747
SPR
1.000 0.200 2 72891502 stop gained A/T snv 8.0E-05 5.6E-05 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs796052505 0.724 0.440 5 162095551 missense variant G/A;C snv 57
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs63750687 0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27