Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8046697 0.925 0.080 16 75408246 intron variant T/C snv 0.51 2
rs12930452 1.000 0.040 16 75428157 intron variant A/G snv 0.51 1
rs2865531 1.000 0.040 16 75356418 intron variant T/A snv 0.52 1
rs3851738 1.000 0.040 16 75353635 intron variant G/A;C snv 1
rs4888378 0.851 0.040 16 75298143 intron variant A/G snv 0.52 1
rs8046696 1.000 0.040 16 75408245 intron variant T/A;G snv 1