Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043397364
DPEP1
1.000 0.080 16 89637349 missense variant G/A;T snv 2.8E-05; 4.0E-06 1
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1044471
ADIPOR2
1.000 0.080 12 1787790 3 prime UTR variant C/T snv 0.38 4
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs1048290
KEAP1
0.851 0.160 19 10489766 synonymous variant G/C snv 0.41 0.48 4
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104893751
OGG1
0.882 0.240 3 9750423 missense variant G/A;C snv 2.2E-03; 4.0E-06 5
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1048945
APEX1 ; OSGEP
0.851 0.120 14 20456008 missense variant G/C snv 2.1E-02 2.4E-02 6
rs10490920
PTEN
1.000 0.080 10 87925886 intron variant T/C snv 0.14 1
rs1049434
SLC16A1
0.925 0.120 1 112913924 missense variant A/T snv 0.59 0.66 2
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10504961
UQCRB
1.000 0.080 8 96227901 3 prime UTR variant C/T snv 0.41 0.46 1
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10