Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74360995 6 21886258 non coding transcript exon variant T/C snv 0.12 1
rs1205896 6 22341240 intron variant G/A snv 0.47 1
rs9393294 6 22465392 intron variant C/T snv 0.13 1
rs12525417 6 22591478 intron variant C/T snv 0.33 1
rs196052 1.000 0.040 6 22056971 intron variant T/A;C snv 1
rs9350395 1.000 0.080 6 21905495 intron variant A/G;T snv 1
rs2744133 6 22392031 intron variant A/G;T snv 1
rs6911827 6 22130372 intron variant C/G;T snv 1
rs9466161 6 21722685 intron variant T/C snv 0.25 1
rs7760082 6 21919156 intron variant G/A snv 0.59 1
rs6934973 6 21920795 intron variant A/G snv 0.32 1
rs13198081 6 22017314 intron variant G/C snv 0.35 1
rs7766436 1.000 0.040 6 22598030 intron variant C/T snv 0.29 1
rs6909752 1.000 0.040 6 22612400 intron variant G/A snv 0.35 1
rs2876643 1.000 0.040 6 22591296 intron variant C/A;T snv 1
rs141007801 6 21722558 intron variant A/-;AA;AAA;AAAA delins 2