Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs2854746
IGFBP3
0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 14
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs767551092
XPC
0.790 0.200 3 14164838 missense variant G/A snv 4.0E-06 10
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs3176352
CDKN1A
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs2274224
PLCE1-AS1 ; PLCE1
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 6
rs104893819
TGFBR2
0.827 0.240 3 30688470 stop gained C/G;T snv 5
rs2273953
TP73
0.851 0.120 1 3682336 5 prime UTR variant G/A;T snv 0.20; 3.3E-04 5
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs756826500
ERCC1
0.925 0.080 19 45413705 missense variant G/A snv 4.0E-06 5
rs11473
BSG
0.882 0.080 19 582982 3 prime UTR variant C/A;T snv 4
rs16845990
ERBB4
0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 4
rs2244438
TRAK2
0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs353163
UBA6-AS1 ; TMPRSS11A
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs756762196
WWOX
0.851 0.120 16 78425054 stop gained C/G;T snv 1.6E-05 4
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3