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
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs746702110
OGG1
0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs17833789 0.807 0.080 17 57153267 intergenic variant C/A snv 0.37 8
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 6
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 5
rs12931267
FANCA
1.000 0.040 16 89752324 intron variant C/G snv 4.7E-02 4
rs1015362 0.925 0.080 20 34150806 regulatory region variant C/T snv 0.42 3
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 3
rs35063026
SPATA33
0.925 0.080 16 89669749 3 prime UTR variant C/T snv 4.7E-02 3
rs1540771
LOC105374875
1.000 0.040 6 466033 intron variant C/A;T snv 2
rs619865
MMP24-AS1-EDEM2 ; MMP24OS ; EIF6
1.000 0.040 20 35279894 intron variant A/G snv 0.94 0.94 2
rs183671
SLC45A2
1.000 0.040 5 33964105 intron variant T/A;G snv 2
rs10444039 1.000 0.040 10 117806027 intergenic variant C/A snv 0.15 1
rs10886142 1.000 0.040 10 117801913 intergenic variant T/C snv 0.47 1
rs4752116 1.000 0.040 10 117823291 downstream gene variant T/C snv 0.72 1
rs10810635
BNC2
1.000 0.040 9 16795243 intron variant T/C snv 9.0E-02 1
rs12259842
HSPA12A
1.000 0.040 10 116695732 intron variant C/G;T snv 1
rs251468
PPARGC1B
1.000 0.040 5 149814922 intron variant C/T snv 0.33 1