Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs1555630216 0.790 0.160 18 10714931 splice acceptor variant C/T snv 22
rs1555648288 0.790 0.160 18 10795003 splice acceptor variant C/T snv 22