Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs2069840 0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs1474348 0.882 0.080 7 22728289 intron variant C/G snv 0.71 4
rs2069832 0.851 0.200 7 22727814 intron variant A/G;T snv 4
rs1554606 0.925 0.120 7 22729088 intron variant T/A;G snv 2
rs2069843
IL6
1.000 0.040 7 22730375 intron variant G/A snv 5.6E-02 1
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 3
rs13306435
IL6
1.000 0.080 7 22731420 missense variant T/A;C snv 2.9E-02; 4.2E-06 1
rs369953112
IL6
1.000 0.040 7 22731416 missense variant T/C snv 1
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1524107 0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02 6
rs2066992 0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02 6
rs2069825 1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05 2
rs1474347 1.000 0.120 7 22728505 non coding transcript exon variant C/A snv 0.69 1
rs2069827 1.000 0.040 7 22725837 non coding transcript exon variant G/C;T snv 1
rs777906302 0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06 3
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04 3
rs2069861
IL6
0.925 0.080 7 22732035 upstream gene variant C/A;T snv 2