Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2116260 1.000 0.080 6 33057663 TF binding site variant T/C snv 8.6E-02 1
rs864622584
APC
1.000 0.080 5 112838623 missense variant G/A snv 1
rs997271472
APC
1.000 0.080 5 112838434 missense variant G/A;T snv 4.0E-06 1
rs9391756
HCG24
1.000 0.080 6 33148017 upstream gene variant C/A;T snv 1
rs3117008
HLA-DPB2
1.000 0.080 6 33128497 intron variant G/A snv 0.43 1
rs3129275
HLA-DPB2
1.000 0.080 6 33126481 intron variant C/T snv 0.40 1
rs4713607
HLA-DPB2
1.000 0.080 6 33123059 intron variant G/A snv 0.43 1
rs140991990
LINC02097 ; SOX9-AS1
1.000 0.080 17 72101710 intron variant A/G snv 5.5E-04 1
rs929783669
STK11
1.000 0.080 19 1220674 missense variant T/C snv 1
rs997363
C2orf83
0.925 0.080 2 227644742 intron variant C/T snv 0.64 2
rs7770370
HLA-DPB1 ; HLA-DPA1
0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27 2
rs3117039
HLA-DPB2
0.925 0.160 6 33118074 intron variant C/T snv 0.35 2
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3
rs180082 0.882 0.080 17 69955727 intergenic variant C/G;T snv 3
rs9302648
AKTIP
0.882 0.080 16 53493869 non coding transcript exon variant G/T snv 0.54 3
rs5757465
APOBEC3G
0.882 0.080 22 39081118 synonymous variant T/C snv 0.37 0.31 3
rs3744935
BCL2
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03 3
rs11079454
BRIP1
0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 3
rs16945692
BRIP1
0.882 0.080 17 61862883 intron variant A/G snv 0.17 3
rs42032
CDK6
0.882 0.080 7 92608112 3 prime UTR variant G/A snv 0.28 3
rs4777498
CELF6
0.882 0.080 15 72285731 3 prime UTR variant C/A snv 0.74 3
rs17885289
CXCL12
0.882 0.080 10 44386212 non coding transcript exon variant C/T snv 0.26 3
rs266093
CXCL12
0.882 0.080 10 44370760 3 prime UTR variant C/G;T snv 3
rs745950347
DAPK1
0.882 0.120 9 87640345 missense variant T/C snv 8.0E-06 3
rs3213172
E2F1
0.882 0.080 20 33677511 missense variant C/T snv 2.4E-05 2.1E-05 3