Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs3219476
MUTYH
0.882 0.200 1 45336998 intron variant A/C snv 0.58 3
rs3219472
TOE1 ; MUTYH
0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs761937143
SMAD4
1.000 0.040 18 51047229 synonymous variant A/C snv 8.0E-06 1
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs8004738
SERPINA1
0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20