Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146795390
EGFR
0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 8
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
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
rs2228059
LOC107984200 ; IL15RA
0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs112290073
TERT
0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4
rs125555
MBD1
0.882 0.080 18 50273809 missense variant G/A;C snv 3.6E-05; 0.19 4
rs1347093
LOC105374690 ; MIR217HG
0.882 0.080 2 56019205 intron variant G/T snv 0.21 4
rs138895564
TERT
0.882 0.080 5 1271959 intron variant C/T snv 5.1E-03 4
rs1397529
GAB1
0.882 0.080 4 143471009 3 prime UTR variant A/C;T snv 4
rs139852726
LPCAT1
0.882 0.080 5 1462734 3 prime UTR variant G/A;C snv 4
rs199905033
IL6ST
0.882 0.080 5 55964205 missense variant G/C snv 4
rs751144688
CD44
1.000 0.080 11 35206195 missense variant C/T snv 4.0E-06 4
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
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