Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071551
HLA-DQB2
1.000 0.080 6 32761682 synonymous variant C/G;T snv 0.67 1
rs2185379
ATG5 ; PRDM1
1.000 0.080 6 106088378 missense variant G/A snv 3.8E-02 4.5E-02 1
rs2213565
HLA-DQA2
1.000 0.080 6 32745411 splice region variant C/T snv 0.81 0.80 1
rs2253705
SFTA2
1.000 0.080 6 30932317 intron variant T/C snv 0.74 1
rs2266963
UBE2L3
1.000 0.080 22 21593178 intron variant C/G snv 0.18 1
rs2301220
HLA-DPA1
1.000 0.080 6 33070989 intron variant C/A;T snv 1
rs2301224
HLA-DPA1
1.000 0.080 6 33070592 intron variant C/A snv 0.28 1
rs2301226
HLA-DPA1
1.000 0.080 6 33066819 non coding transcript exon variant G/A snv 0.16 1
rs2308911
HLA-DPA1
1.000 0.080 6 33069803 missense variant T/G snv 0.23 0.28 1
rs2395223 1.000 0.080 6 32614001 intergenic variant C/T snv 0.44 1
rs2395535 1.000 0.080 6 32689574 TF binding site variant A/C;G snv 1
rs2567279
HLA-DPA1 ; HLA-DPB1
1.000 0.080 6 33078885 intron variant T/C snv 0.27 1
rs2646996 1.000 0.080 6 32697964 intergenic variant A/G snv 0.34 1
rs2647047 1.000 0.080 6 32700927 regulatory region variant C/G snv 0.34 1
rs2708973 1.000 0.080 2 112906296 intergenic variant A/G snv 0.96 1
rs2836389
ERG
1.000 0.080 21 38431740 intron variant T/C snv 0.27 1
rs28452918
HLA-DPA1
1.000 0.080 6 33071518 intron variant T/A snv 0.29 1
rs2854028
RING1
1.000 0.080 6 33211912 missense variant C/A;T snv 2.7E-05; 0.22 1
rs2856664 1.000 0.080 6 32697839 intergenic variant G/T snv 0.34 1
rs2856704 1.000 0.080 6 32703237 downstream gene variant C/A snv 0.34 1
rs2856720 1.000 0.080 6 32700880 regulatory region variant C/T snv 0.34 1
rs2856822
RPL32P1 ; HLA-DPA1 ; HLA-DPB1
1.000 0.080 6 33079655 non coding transcript exon variant A/C snv 0.41 1
rs2858859 1.000 0.080 6 32614498 intergenic variant G/A snv 0.43 1
rs2894316 1.000 0.080 6 33098817 upstream gene variant A/G snv 0.57 1
rs3091281
HLA-DPB1
1.000 0.080 6 33088789 3 prime UTR variant T/C snv 0.25 1