Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs199469465 0.672 0.560 16 30737343 stop gained C/A;T snv 50
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23