Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60652225 0.851 0.200 1 156130679 missense variant T/C;G snv 4
rs121912496 0.882 0.120 1 156134910 missense variant C/G;T snv 3
rs267607545 0.882 0.200 1 156136121 missense variant G/A;C;T snv 3
rs267607594 0.925 0.120 1 156130745 missense variant T/C snv 3
rs267607639 0.882 0.200 1 156136939 missense variant T/C snv 3
rs28928901 0.882 0.120 1 156134829 missense variant C/T snv 3
rs28933090 0.925 0.160 1 156115172 missense variant T/A;G snv 3
rs58850446 0.925 0.200 1 156134908 missense variant T/C snv 3
rs60934003 0.882 0.160 1 156137213 missense variant T/C snv 3
rs267607613 0.925 0.120 1 156137678 missense variant C/T snv 7.0E-06 2
rs267607634 0.925 0.120 1 156136045 missense variant G/A;C snv 2
rs267607637 0.925 0.120 1 156136402 missense variant G/A snv 2
rs57207746 0.925 0.120 1 156134860 missense variant G/A snv 2
rs57747780 0.925 0.200 1 156136981 missense variant T/C snv 2
rs58436778 0.925 0.120 1 156115052 missense variant A/G snv 2
rs58917027 1.000 0.120 1 156130708 missense variant A/C;G snv 2
rs59653062 0.925 0.120 1 156136076 missense variant T/A snv 2
rs61094188 0.925 0.160 1 156136257 missense variant C/A;T snv 7.6E-05 2
rs61295588 0.925 0.160 1 156134809 missense variant T/C snv 2
rs13768 1.000 0.120 1 156138660 missense variant G/A;T snv 2.4E-05 1
rs1553265999 1.000 0.120 1 156136925 missense variant A/C snv 1
rs267607614 1.000 0.120 1 156115016 missense variant A/G snv 1
rs267607629 1.000 0.120 1 156134507 missense variant C/G snv 1
rs267607630 1.000 0.120 1 156134967 missense variant T/C snv 1
rs267607633 1.000 0.120 1 156135259 missense variant T/C snv 1