Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 4
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 3
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 3
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs2856437
PBX2
1.000 0.120 6 32189587 intron variant G/A snv 3.7E-02 3
rs2858310 1.000 0.120 6 32700546 TF binding site variant G/A snv 0.64 3
rs3132947
NOTCH4
1.000 0.120 6 32209005 intron variant G/T snv 0.19 3
rs4272
CDK6
1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv 3
rs589428
SLC44A4 ; CYP21A2 ; EHMT2 ; LOC107986588 ; EHMT2-AS1
1.000 0.120 6 31880443 non coding transcript exon variant T/G snv 0.77 3
rs6928482
HLA-DQB1-AS1
1.000 0.120 6 32658472 upstream gene variant T/C snv 0.47 3
rs7573065
SLC11A1
1.000 0.120 2 218381984 upstream gene variant C/A;T snv 3
rs8192575
NOTCH4
1.000 0.120 6 32198607 intron variant C/G;T snv 7.0E-02; 4.1E-06 3
rs9275292 1.000 0.120 6 32695512 intergenic variant C/A snv 0.53 3
rs1033500
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32339605 missense variant G/A snv 0.40 0.33 2
rs1046080
PRRC2A
1.000 0.120 6 31628105 missense variant C/A snv 0.79 0.74 2
rs11089637 1.000 0.120 22 21624807 downstream gene variant T/C snv 0.28 2
rs1133104
CLEC4A
1.000 0.120 12 8138526 3 prime UTR variant T/G snv 0.25 2
rs140142800 1.000 0.120 10 61036479 regulatory region variant C/T snv 2.2E-02 2
rs1403155 1.000 0.120 7 68585426 intergenic variant G/A snv 2.9E-02 2
rs1474728
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32334290 intron variant C/T snv 0.33 2
rs150110 1.000 0.120 6 167098278 intron variant G/A snv 0.71 2
rs1502644 1.000 0.120 5 3670892 intergenic variant C/A snv 0.85 2
rs1877030 1.000 0.120 17 39583908 intergenic variant T/C snv 0.81 2