Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs177430 18 23506161 intron variant C/A;T snv 4
rs1808579 18 23524924 intron variant C/T snv 0.47 3
rs891387 18 23523945 intron variant T/C snv 0.55 2
rs1788808 18 23510059 intron variant A/C;G snv 1
rs1788820 18 23521980 intron variant A/G snv 0.69 1