Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61863282 10 97591247 intron variant C/T snv 0.11 1
rs11817730 10 97598754 intron variant A/G snv 0.18 0.20 1
rs2297644 10 97599982 non coding transcript exon variant T/C snv 0.15 1
rs7068278 10 97597385 intron variant G/T snv 0.18 1
rs7078003 10 97599655 non coding transcript exon variant C/T snv 0.14 0.14 1
rs7913812 10 97597874 intron variant T/C snv 0.20 1
rs2861970 10 97592327 intron variant A/C;G;T snv 1