Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1007934 14 72996771 intron variant G/A snv 0.33 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3
rs1349265 1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv 2