Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749836 0.827 0.160 14 73192786 missense variant G/A snv 5
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 5
rs63751223 0.807 0.160 14 73219161 missense variant G/C snv 5
rs1566650594 0.851 0.120 14 73206384 splice acceptor variant A/T snv 4
rs63749824 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 4
rs63750053 0.827 0.120 14 73192721 missense variant G/T snv 4
rs63750082 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 4
rs63750083 0.732 0.160 14 73219177 missense variant C/A;T snv 4
rs63750450 0.851 0.120 14 73173571 missense variant A/G snv 4
rs63750526 0.776 0.160 14 73192832 missense variant C/A snv 4
rs63750590 0.790 0.120 14 73186860 missense variant A/G snv 4
rs63750900 0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 4
rs63751278 0.827 0.120 14 73173631 missense variant A/G snv 4
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 4
rs661 0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 4
rs63751068 0.827 0.120 14 73186920 missense variant G/C;T snv 2
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 1