Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753625117 1.000 0.080 2 98396125 missense variant T/C snv 1.6E-05 7.0E-06 1
rs1568626209
CRX
1.000 0.080 19 47839569 frameshift variant G/- del 1
rs281865516
CRX
1.000 0.080 19 47839678 frameshift variant C/- delins 1
rs1415160006
EYS ; PHF3
1.000 0.080 6 63720689 missense variant A/T snv 7.0E-06 1
rs61750178 1.000 0.080 17 8015031 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 1
rs1186374130 1.000 0.080 12 110209209 missense variant T/C snv 8.2E-06 1
rs546724699 1.000 0.080 12 110180446 stop gained C/T snv 4.1E-06 3.5E-05 1
rs796051882 1.000 0.080 4 15988237 intron variant T/C snv 7.0E-06 1
rs794727903 0.925 0.080 1 94080697 stop gained G/A snv 2
rs137853190
EYS ; PHF3
0.925 0.080 6 63720626 stop gained A/T snv 1.6E-05 2
rs373032226 0.925 0.080 14 67727062 missense variant C/T snv 9.5E-05 2.8E-05 2
rs1410483989 0.925 0.120 15 90433737 missense variant A/G snv 4.0E-06 7.0E-06 2
rs786200944 0.925 0.080 4 13376553 stop gained G/A;T snv 2
rs149672683
SP4
0.925 0.080 7 21430082 missense variant A/G snv 1.8E-02 6.5E-03 2
rs61749414 0.882 0.080 1 94062611 stop gained G/A;T snv 3
rs104894672
CRX
0.882 0.080 19 47836263 missense variant C/T snv 8.0E-06 3
rs61748459
CRX
0.882 0.080 19 47839791 missense variant G/A snv 1.2E-03 5.1E-03 3
rs146705250
ERG
0.882 0.080 21 38403679 missense variant C/T snv 8.0E-06 4.2E-05 3
rs1234399841 0.882 0.080 2 61839728 missense variant A/C snv 4.0E-06 3
rs61750174 0.882 0.080 17 8014704 missense variant C/A;G;T snv 4.0E-06; 1.6E-05; 4.0E-06 3
rs62645932 0.882 0.080 6 42704594 missense variant A/T snv 3
rs398123044 0.882 0.080 4 13381577 stop gained G/A;C;T snv 8.0E-06; 4.0E-06; 4.0E-06 3
rs28942109 0.882 0.160 5 134608443 missense variant C/T snv 2.4E-05 3.5E-05 3
rs1024983534 0.882 0.080 5 1294569 missense variant C/G snv 7.0E-06 3
rs1060503013 0.882 0.080 5 1294844 missense variant G/A;C snv 1.5E-05 3