Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs3087399
REV1
0.882 0.120 2 99438696 missense variant T/C snv 0.13 0.17 4
rs8038415
IGF1R
15 98956205 intron variant T/C snv 0.58 1
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 7
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs746702110
OGG1
0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs7015700
TNKS
1.000 0.080 8 9670197 splice donor variant G/A snv 0.23 2
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10