Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412444 0.851 0.120 10 89243170 intron variant C/T snv 0.37 2
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs2246942 0.925 0.040 10 89245129 intron variant A/C;G snv 1