Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs3790622
IL19 ; IL10
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3