Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs1057519696
ALK
1.000 0.040 2 29214054 missense variant C/T snv 5
rs751144688
CD44
1.000 0.080 11 35206195 missense variant C/T snv 4.0E-06 4
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs586339
KDM4A
1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs7015700
TNKS
1.000 0.080 8 9670197 splice donor variant G/A snv 0.23 2
rs764664272
MMP2
1.000 0.120 16 55484060 missense variant A/G snv 1.2E-05 7.0E-06 2
rs766779326
ESR1
1.000 0.040 6 151944344 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
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
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs3660
KRT86 ; KRT81
0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6
rs2228059
LOC107984200 ; IL15RA
0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs112290073
TERT
0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4