Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7097656 0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs6586030 1.000 0.040 10 80494291 intron variant A/G;T snv 2
rs1993484 10 80462942 intron variant T/C snv 0.82 1
rs7086627 10 80460841 intron variant C/T snv 0.80 1
rs7100689 10 80462422 intron variant C/A;G snv 1
rs12220642 10 80459208 intron variant T/C;G snv 1
rs1902661 1.000 0.040 10 80458350 intron variant G/A;C snv 1
rs10788639 10 80473469 intron variant C/G snv 0.64 1
rs17680741 1.000 0.040 10 80491758 intron variant T/C snv 0.25 1
rs12264252 1.000 0.040 10 80517585 intron variant G/A snv 0.18 1