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
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
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs10420685
ITPKC
1.000 0.080 19 40729215 synonymous variant A/G snv 7.2E-02 9.7E-02 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
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs2229546
IL12RB2
1.000 0.080 1 67395837 synonymous variant C/A;G;T snv 0.63; 1.2E-05; 2.4E-05 1
rs2229634
ITPR3
0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs12494623
PIK3CA
1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs16997517
CSF2RB
0.925 0.200 22 36937894 missense variant C/T snv 2.6E-02 4.7E-02 2
rs3748079
ITPR3
0.925 0.160 6 33620370 5 prime UTR variant C/T snv 0.18 2