Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 10
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs1063169
FOS
0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12 2
rs1064795747
MSH2
0.925 0.080 2 47412433 missense variant T/C snv 4
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs1065411
GSTM2 ; GSTM1
0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 2
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10845671
GPRC5D-AS1
0.925 0.080 12 12926708 upstream gene variant C/A;T snv 2
rs10883782
WBP1L
0.925 0.080 10 102824175 intron variant A/G snv 0.14 2
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691029
TP53
0.827 0.160 17 7673794 missense variant C/G snv 6
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70