Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2067087 1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs1859168 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs3735533 7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs4722675 7 27204343 intron variant A/G snv 0.93 4
rs2023843 7 27203602 intron variant C/T snv 0.90 2
rs60772526 7 27206377 non coding transcript exon variant C/G;T snv 1