Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs377274761 0.776 0.240 14 87968393 missense variant C/T snv 8.0E-06 2.8E-05 20
rs1057518843 0.790 0.240 14 87988523 missense variant C/T snv 19
rs886041091 0.807 0.120 9 84751990 missense variant A/G snv 18
rs142285818
RHO
0.807 0.120 3 129532727 missense variant C/G;T snv 9.7E-04 4.1E-04 11
rs864309505 0.807 0.200 11 6615220 missense variant T/G snv 10
rs386834061 0.925 0.360 8 99868312 stop gained C/T snv 2.1E-05 10
rs1057518939 1.000 0.040 8 99511424 frameshift variant A/- del 9
rs1561416879 0.925 0.200 5 90629308 stop gained C/G snv 6
rs1564855725 0.882 0.160 11 6617621 splice region variant C/T snv 5
rs606231180 0.925 0.080 X 38285902 frameshift variant CC/- delins 3