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
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs1562846694 0.763 0.320 7 100643252 inframe deletion TTCGCTCCACGCACT/- delins 32