Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174574 1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs2072114 1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18