Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852584
AR
0.925 0.080 X 67711459 missense variant G/A snv 2
rs139756052
AR
0.925 0.080 X 67643314 missense variant A/T snv 1.3E-04 5.6E-04 2
rs17302090 0.925 0.080 X 67535561 downstream gene variant G/A snv 8.5E-02 2
rs2315123
OPN1LW
0.925 0.080 X 154156372 missense variant T/C;G snv 5.5E-06 2
rs2405942
SHROOM2
0.925 0.080 X 9846095 intron variant G/A snv 2
rs5945372
PNMA6E ; LOC105373379
0.925 0.080 X 153400456 intron variant A/C;T snv 2
rs777787518
AR
0.925 0.080 X 67545298 missense variant G/A snv 2
rs138454018
AR
1.000 0.080 X 67546171 missense variant C/A;T snv 4.4E-05; 4.9E-05 1
rs1419040 1.000 0.080 X 51609183 intergenic variant G/A snv 1
rs4604628 1.000 0.080 X 51644318 intergenic variant C/G;T snv 1
rs5991735
MAGED1
1.000 0.080 X 51809788 intron variant G/A;C snv 1
rs78686797
AR
1.000 0.080 X 67545316 missense variant T/A snv 1.1E-03 1
rs868669253
AR
1.000 0.080 X 67711405 missense variant G/A;T snv 1
rs985081 1.000 0.080 X 149456568 intergenic variant T/C snv 0.14 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs555607708
CHEK2
0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs137853011
CHEK2
0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 16
rs778212685
CHEK2
0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs121908698
CHEK2
0.851 0.200 22 28725242 splice donor variant C/A;T snv 4.0E-06; 1.3E-04 7
rs72552322
CHEK2
0.925 0.120 22 28725070 missense variant C/T snv 2.4E-05 7.0E-06 7
rs730881701
CHEK2
0.827 0.200 22 28725278 stop gained G/A;C snv 2.4E-05 7.0E-06 6
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs200917541
CHEK2
0.851 0.200 22 28725270 stop gained G/A;T snv 5