Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2517955 1.000 0.080 17 39687428 intron variant C/T snv 0.51 1
rs12150298 1.000 0.080 17 39678288 intron variant T/C snv 0.58 1
rs1565922 1.000 0.080 17 39674782 intron variant A/G;T snv 1
rs2941503 1.000 0.080 17 39672492 missense variant A/G snv 0.64 1
rs2941504 1.000 0.080 17 39674647 synonymous variant A/G snv 0.67 0.64 1