Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10037512 5 89058858 intron variant T/A;C snv 2
rs10901216 9 130596504 intron variant G/A snv 0.28 2
rs118115924 12 48985754 downstream gene variant G/A;T snv 2
rs1366594 5 89080244 intron variant A/C snv 0.57 2
rs4580892 6 127088737 intron variant C/T snv 0.32 2
rs6894139 5 89031965 non coding transcript exon variant T/G snv 0.57 2
rs6959212 7 38088724 intergenic variant T/C;G snv 2
rs7466269 9 130588697 intron variant A/G snv 0.33 2
rs9921222 0.925 0.120 16 325782 intron variant C/T snv 0.51 2