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
rs1333047 0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs4380028 0.807 0.120 15 78818751 intron variant C/T snv 0.34 7
rs4731702 0.925 0.120 7 130748625 intergenic variant C/T snv 0.40 5