Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs4845384
ADAR
1.000 0.080 1 154615193 intron variant A/G snv 0.69 1
rs76844316
BTLA
1.000 0.080 3 112469762 missense variant T/G snv 2.4E-02 2.2E-02 1
rs78900671
COL22A1
1.000 0.080 8 138653967 intron variant G/A;C snv 1
rs2617160
KLRC4-KLRK1 ; LOC101928100
1.000 0.080 12 10392998 intron variant A/C;T snv 1
rs4935047
MBL2
1.000 0.080 10 52770307 intron variant A/G snv 0.49 1
rs9287655
NBAS
1.000 0.080 2 15245360 intron variant C/T snv 0.45 1
rs61886277
PLCE1
1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 1
rs7712322
POLR3G
1.000 0.080 5 90482078 intron variant C/A;T snv 1
rs378352
HLA-DOA
0.925 0.200 6 33007157 synonymous variant G/A;C snv 0.20 2
rs9366816
HLA-DPA3 ; LOC105375021
0.925 0.080 6 33136398 intron variant T/C snv 0.22 2
rs3806798
IL15
0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 2
rs12354
LTBR
0.925 0.080 12 6390939 3 prime UTR variant T/A;G snv 1.6E-04; 0.76 2
rs2132039
UGT2B28
0.925 0.120 4 69293669 intron variant T/A;C snv 2
rs148314165 0.925 0.160 6 137908902 intergenic variant T/- delins 2.0E-02 3
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs9276370
HLA-DQA2
0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 3
rs117648444
IFNL4
0.882 0.160 19 39247938 missense variant G/A snv 0.25 8.1E-02 3
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs7095891
MBL2
0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 3
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs9277542
HLA-DPB1
0.851 0.280 6 33087470 3 prime UTR variant T/A;C snv 4
rs7756516
HLA-DQB2
0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 4