Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 1
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 1
rs17033
ADH1B
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02 1
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs16260
CDH1
0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 1
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 1
rs780759537
CDH1
1.000 0.080 16 68822082 missense variant G/A snv 1.6E-05 4.2E-05 1
rs465498
CLPTM1L
0.776 0.200 5 1325688 non coding transcript exon variant A/G snv 0.46 1
rs869736
CORO1B ; PTPRCAP
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53 1
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31 1
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 1
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 1
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 1
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs2854746
IGFBP3
0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 1
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1135354
IL18R1
0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 1