Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1554121443 0.742 0.280 6 33438873 stop gained C/T snv 29
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs1555429629 0.763 0.200 15 40729632 missense variant G/A snv 23