Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs3754093
EXO1
0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs369410616
MUTYH
0.752 0.280 1 45329400 missense variant C/T snv 2.0E-05 2.8E-05 10
rs1635498
EXO1
0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs1776148
EXO1
0.807 0.160 1 241879243 missense variant A/G snv 0.66 0.66 9
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs751763046
EXO1
0.790 0.200 1 241885375 missense variant T/C snv 4.0E-06 8
rs3219484
MUTYH
0.807 0.160 1 45334484 missense variant C/A;T snv 4.8E-02 4.8E-02 7
rs768873896
MTHFR
0.790 0.160 1 11794822 missense variant C/G;T snv 8.0E-06; 2.4E-05 7
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs538874513
TP73
0.807 0.120 1 3730017 missense variant C/G;T snv 8.2E-06; 8.2E-06 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs228729
PER3
0.827 0.120 1 7785635 intron variant T/C snv 0.69 0.69 5
rs3134615
MYCL-AS1 ; MYCL
0.827 0.120 1 39896394 3 prime UTR variant C/A snv 0.17 5
rs3842530
MIR205 ; MIR205HG
0.827 0.120 1 209432292 non coding transcript exon variant GCAGCAGCAGCAGCAGCAGCAGCAGCA/-;GCA;GCAGCA;GCAGCAGCA;GCAGCAGCAGCA;GCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA delins 5
rs533748068
ARHGEF2 ; MIR6738
0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs758244932
EPHX1
0.827 0.120 1 225828842 missense variant C/T snv 1.3E-04 1.0E-04 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs1060501327
MUTYH
0.851 0.080 1 45332251 missense variant A/G snv 4
rs12072037
MFSD2A
0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4