Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24