Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1356083197
CNIH3 ; WDR26
1.000 0.040 1 224434068 missense variant C/T snv 1.5E-05 1.4E-05 2
rs1374712964
MUTYH
1.000 0.080 1 45332028 missense variant T/C snv 2
rs587776946
LRIG2
1.000 1 113114471 stop gained C/T snv 2
rs1261963959
KIF1B
1 10297069 missense variant G/A snv 4.0E-06 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs4987188
MSH2
0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31 9
rs2303426
MSH2
0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs772399455
MYCNOS ; MYCN
0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs121912518
LHCGR ; STON1-GTF2A1L ; GTF2A1L
0.882 0.160 2 48688064 missense variant T/C;G snv 5