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
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14