Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 10
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs2303426
MSH2
0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs4595552 0.790 0.080 11 125865825 intergenic variant C/G;T snv 7
rs775066324
TIMP2
0.790 0.080 17 78855710 missense variant G/A;C snv 4.0E-06; 4.0E-06 7
rs779162432
PPIG
0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 7
rs909629195
LASP1 ; MIR6779
0.790 0.080 17 38914448 missense variant C/T snv 7
rs951540403
PLCE1
0.790 0.080 10 94132433 missense variant G/C snv 7
rs1444424830
FASTK
0.790 0.080 7 151078923 missense variant C/T snv 4.6E-06 7.0E-06 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs746702110
OGG1
0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs778985185
EGFR
0.851 0.160 7 55163734 missense variant G/A snv 8.0E-06 3.5E-05 5
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs6259
SHBG
0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1157
ALCAM
0.790 0.080 3 105576617 3 prime UTR variant G/A snv 0.16 7
rs2486758
CYP17A1
0.742 0.160 10 102837723 upstream gene variant T/C snv 0.18 11
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2072668
OGG1
0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14