Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1610588 1.000 0.120 6 29708939 upstream gene variant C/T snv 0.19 1
rs1610742 1.000 0.120 6 29710175 upstream gene variant T/C snv 0.19 1
rs232228 1.000 0.120 2 88859459 intron variant G/A snv 0.15 1
rs2735845 1.000 0.120 5 1300469 intergenic variant C/G snv 0.16 1
rs29218 1.000 0.120 6 29639652 upstream gene variant A/G snv 0.17 1
rs3095267 1.000 0.120 6 29639269 upstream gene variant G/C;T snv 1
rs3095341 1.000 0.120 6 30758971 intron variant T/C snv 0.69 1
rs3131866 1.000 0.120 6 29703963 downstream gene variant G/A snv 0.24 1
rs533550179 1.000 0.120 6 29714462 intergenic variant C/T snv 1
rs577078190 1.000 0.120 6 29716031 intergenic variant G/A snv 1
rs9258122 1.000 0.120 6 29703963 downstream gene variant G/A snv 1
rs3928672
AGO2
1.000 0.120 8 140562068 intron variant C/A;T snv 1
rs4771436
BIVM-ERCC5 ; ERCC5
1.000 0.120 13 102849670 intron variant T/G snv 0.22 1
rs1407019
BPIFA1
1.000 0.120 20 33237991 intron variant G/A snv 0.27 1
rs2752903
BPIFA1
1.000 0.120 20 33235584 upstream gene variant T/C;G snv 0.33 1
rs750064
BPIFA1
1.000 0.120 20 33235824 upstream gene variant T/A;C snv 1
rs7252229
CD209
1.000 0.120 19 7747295 intron variant G/C snv 0.14 0.22 1
rs115214213
CD44
1.000 0.120 11 35231896 3 prime UTR variant T/C snv 4.9E-03 1
rs3740194
CELF2
1.000 0.120 10 11255346 intron variant T/C snv 0.47 1
rs1536826
CYP2E1
1.000 0.120 10 133543735 intron variant A/C snv 0.62 1
rs8192780
CYP2E1
1.000 0.120 10 133540621 intron variant T/G snv 0.64 1
rs3827688
CYP2E1 ; SYCE1
1.000 0.120 10 133555754 non coding transcript exon variant C/T snv 0.13 9.4E-02 1
rs1059449
HLA-A
1.000 0.120 6 29942921 missense variant G/A snv 6.1E-02 9.0E-02 1
rs2975042
HLA-A
1.000 0.120 6 29952759 upstream gene variant G/A;T snv 1
rs3869062
HLA-A
1.000 0.120 6 29967114 downstream gene variant A/G snv 5.5E-02 1