Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs1250557 1.000 0.080 10 79306017 intron variant G/T snv 0.63 1