Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs777787518
AR
0.925 0.080 X 67545298 missense variant G/A snv 2
rs140659849
DGKK
1.000 0.080 X 50451939 intron variant G/A snv 5.6E-03 1
rs17321482
ARHGAP6
1.000 0.080 X 11464514 intron variant C/T snv 9.0E-02 1
rs2788524
ARHGAP6
1.000 0.080 X 11321091 intron variant G/A snv 0.12 1
rs2807031
XAGE3
1.000 0.080 X 52867918 intron variant T/C snv 0.18 1
rs4826594 1.000 0.080 X 54427973 regulatory region variant G/A snv 0.21 1
rs4844289
LOC107985688
1.000 0.080 X 71188133 intron variant A/G snv 0.51 1
rs6625711 1.000 0.080 X 70920000 intergenic variant A/G;T snv 1
rs723557 1.000 0.080 X 127519376 intergenic variant T/G snv 7.2E-02 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
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs778212685
CHEK2
0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs587780170
CHEK2
0.851 0.120 22 28695786 missense variant C/A;G;T snv 2.8E-05; 8.0E-06 5
rs786203472
CHEK2
0.827 0.120 22 28719414 start lost T/C snv 5
rs863224748
CHEK2
0.827 0.120 22 28734721 start lost T/C snv 5
rs200050883
CHEK2
0.851 0.120 22 28695190 missense variant C/A;G;T snv 3.9E-04 3.4E-04 4
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 4
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38 4
rs11704416
FAM83F
0.925 0.080 22 40040969 3 prime UTR variant G/C snv 0.21 2
rs11913319
TXNRD2
0.925 0.080 22 19880016 intron variant C/G snv 0.26 2
rs138708
SUN2
0.925 0.080 22 38742327 missense variant G/A;T snv 2.2E-02; 4.0E-06 2
rs16982844
COMT
0.925 0.080 22 19960419 intron variant C/A snv 4.3E-02 2
rs17886163
CHEK2
0.925 0.080 22 28695159 missense variant A/C snv 1.4E-03 5.4E-03 2