Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs28493229
ITPKC ; COQ8B
0.925 0.200 19 40718299 intron variant G/A;C snv 6.0E-06; 0.12 3
rs12494623
PIK3CA
1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs3024656
IL4R
1.000 0.080 16 27358288 intron variant G/A snv 0.20 1
rs3181224
LOC105377683
1.000 0.080 5 159313842 intron variant A/G snv 0.10 1
rs3729679
PIK3CA
1.000 0.080 3 179204642 intron variant A/G snv 0.58 1
rs853360
CD83
1.000 0.080 6 14134361 intron variant T/C snv 0.74 1
rs2029167
LOC105369777
0.925 0.080 12 54196349 intergenic variant G/A snv 0.52 3
rs2029166
LOC105369777
1.000 0.080 12 54196315 intergenic variant C/T snv 0.33 1
rs7296239
LOC105369777
1.000 0.080 12 54197920 intergenic variant T/C snv 0.42 1
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs750553272
NFE2L2
0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs16997517
CSF2RB
0.925 0.200 22 36937894 missense variant C/T snv 2.6E-02 4.7E-02 2
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62