Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs17239025 1.000 0.080 13 30765768 downstream gene variant G/C snv 4.1E-02 1
rs17268122
ABCC4
1.000 0.080 13 95192240 intron variant G/A;C;T snv 2
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799929
NAT2
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs1801673
ATM
0.882 0.120 11 108304736 missense variant A/T snv 4.9E-03 4.4E-03 3
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1970764
PPP1R13L
0.851 0.120 19 45387615 intron variant T/C snv 0.27 4
rs202195689
MIR4274 ; SORCS2
1.000 0.080 4 7460097 mature miRNA variant -/C;CACCC;CCC delins 1
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs2072749
SELENON
1.000 0.080 1 25804530 intron variant T/C snv 0.23 1
rs2073438
ALOX12 ; ALOX12-AS1
0.925 0.160 17 6996757 intron variant G/A snv 0.20 2