Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs369160589 0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04 35
rs1009298200 0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06 34
rs1555452127 0.742 0.400 16 5079078 missense variant T/C snv 34