Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs928674
LAMC3
0.827 0.080 9 131076637 intron variant A/G snv 0.16 6
rs9879992
GSK3B
0.882 0.120 3 119993874 intron variant A/G snv 0.28 4
rs1950252
BCL2L2-PABPN1 ; BCL2L2
1.000 0.080 14 23309489 3 prime UTR variant A/G snv 0.93 2
rs3757769
SND1
1.000 0.080 7 127901009 intron variant A/G snv 9.7E-02 2
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs334348
TGFBR1
0.851 0.160 9 99150189 3 prime UTR variant A/G;T snv 5
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs1406
CCNE1
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28 4
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs1635498
EXO1
0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28903081
KLC1 ; XRCC3
0.851 0.200 14 103698934 missense variant C/A;T snv 4.5E-06; 4.3E-04 5
rs1816158
MIR100HG
0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79