Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13361707 0.882 0.120 5 40791782 intron variant C/T snv 0.31 6
rs10074991 0.851 0.120 5 40790449 intron variant G/A snv 0.31 5
rs154268 0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs461404 0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs3805490 0.925 0.080 5 40792051 intron variant T/A snv 0.21 2
rs6882903 0.925 0.080 5 40765760 intron variant A/C snv 2.7E-03 2