Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800553
ABCA4
0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs76216585
POC1B
0.807 0.160 12 89492071 stop gained C/A;G;T snv 8.5E-06; 2.7E-04 9
rs768435443
ABCA4
0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 8
rs104894673
CRX
0.776 0.160 19 47839335 missense variant C/T snv 2.1E-05 8
rs104893968
GUCA1A
0.790 0.200 6 42173762 missense variant C/G;T snv 4.0E-06; 1.2E-03 8
rs61750172
GUCY2D
0.807 0.080 17 8014700 missense variant C/A;T snv 4.0E-06 8
rs121434631
GUCA1A
0.807 0.080 6 42179248 missense variant C/G;T snv 4.0E-06 6
rs61750173
GUCY2D
0.827 0.080 17 8014701 missense variant G/A snv 6
rs281865404
ABCA4
0.851 0.080 1 94014675 missense variant GG/CA mnv 4
rs104894671
CRX
0.851 0.080 19 47836381 missense variant A/C snv 4
rs61748436
CRX
0.851 0.080 19 47836264 missense variant G/A snv 1.4E-05 4
rs28933695
GUCY2D
0.851 0.080 17 8014699 missense variant G/C snv 4
rs61755815
PRPH2
0.851 0.080 6 42704463 missense variant T/G snv 4
rs62645926
PRPH2
0.851 0.080 6 42721784 missense variant T/G snv 4
rs759999855
RIMS1
0.851 0.080 6 72392784 missense variant G/A snv 4.0E-06 4
rs200707391
CC2D2A
0.882 0.160 4 15557452 missense variant G/A;C;T snv 1.7E-04; 4.1E-06; 1.2E-05 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
FAM161A
0.882 0.080 2 61839728 missense variant A/C snv 4.0E-06 3
rs61750174
GUCY2D
0.882 0.080 17 8014704 missense variant C/A;G;T snv 4.0E-06; 1.6E-05; 4.0E-06 3
rs202210819
KIZ
0.882 0.080 20 21136463 stop gained C/T snv 4.9E-04 3.1E-04 3
rs62645932
PRPH2
0.882 0.080 6 42704594 missense variant A/T snv 3
rs104893782
RHO
0.882 0.080 3 129532340 missense variant T/G snv 3
rs1024983534
TERT
0.882 0.080 5 1294569 missense variant C/G snv 7.0E-06 3