Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
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
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs727088
CD226
0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 8
rs4705343
MIR143 ; CARMN
0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
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
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs2029167
LOC105369777
0.925 0.080 12 54196349 intergenic variant G/A snv 0.52 3
rs3748079
ITPR3
0.925 0.160 6 33620370 5 prime UTR variant C/T snv 0.18 2
rs12494623
PIK3CA
1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs2029166
LOC105369777
1.000 0.080 12 54196315 intergenic variant C/T snv 0.33 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