Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587778883
MLH1
0.807 0.200 3 37025648 frameshift variant A/- del 7
rs762581936
MUC4
0.827 0.240 3 195788569 missense variant C/G;T snv 1.1E-05; 1.1E-05 5
rs56053615
OGG1
0.851 0.120 3 9751845 missense variant G/A;T snv 3.4E-04; 4.0E-06 4
rs587778992
MLH1
0.882 0.200 3 37050606 stop gained C/T snv 4
rs752967378
RAF1
0.882 0.160 3 12618580 missense variant G/A;C snv 4.0E-06 3
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2
rs3731114
XPC
0.925 0.120 3 14165122 intron variant C/G snv 1.8E-02 2
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs782095550
MANF
0.925 0.120 3 51386267 missense variant T/C snv 2
rs1447826 1.000 0.120 3 74669607 intergenic variant T/A;C;G snv 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12