Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs11064
TNFAIP8
0.807 0.120 5 119393693 3 prime UTR variant A/G snv 0.27 9
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs13405728
STON1-GTF2A1L ; LHCGR
0.790 0.200 2 48751020 intron variant A/G snv 0.15 8
rs3819102
ENOSF1
0.827 0.120 18 675307 intron variant A/G snv 4.5E-02 3.6E-02 8
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs2479106
DENND1A
0.851 0.120 9 123762933 intron variant A/G snv 0.44 4
rs397517202
PIK3CA
0.851 0.320 3 179234230 missense variant A/G snv 4
rs1045242
TNFAIP8
0.925 0.080 5 119393632 3 prime UTR variant A/G snv 0.32 3
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3
rs17601876
MIR4713HG ; CYP19A1
1.000 0.080 15 51261712 intron variant A/G snv 0.58 3
rs11263761
HNF1B
1.000 0.080 17 37737784 intron variant A/G snv 0.44 2
rs3741211
INS-IGF2 ; IGF2 ; IGF2-AS
0.925 0.080 11 2147880 non coding transcript exon variant A/G snv 0.36 2
rs6782972
RARB
0.925 0.080 3 24922859 intron variant A/G snv 0.31 2
rs771432878
CYP1A1
0.925 0.080 15 74723013 missense variant A/G snv 4.0E-06 3.5E-05 2
rs79575945
ESR1
0.925 0.080 6 151837712 intron variant A/G snv 7.9E-02 2
rs12184995
LINC02331 ; LOC105370504
1.000 0.080 14 53759970 intron variant A/G snv 0.83 1
rs2797160
LINC02523 ; LOC105377986
1.000 0.080 6 125688970 intron variant A/G snv 0.48 1