Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs801114 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 5
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs4771436
BIVM-ERCC5 ; ERCC5
1.000 0.120 13 102849670 intron variant T/G snv 0.22 1
rs8192780
CYP2E1
1.000 0.120 10 133540621 intron variant T/G snv 0.64 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1760944
OSGEP ; APEX1
0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 5
rs884225
EGFR
0.827 0.160 7 55206391 3 prime UTR variant T/C;G snv 5
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 3
rs2752903
BPIFA1
1.000 0.120 20 33235584 upstream gene variant T/C;G snv 0.33 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16