Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs61755792
PRPH2
0.763 0.160 6 42721821 missense variant G/A;C snv 10
rs29001566
RHO
0.807 0.080 3 129533711 missense variant C/A;G;T snv 10
rs104893775
RHO
0.807 0.160 3 129530917 missense variant C/T snv 7
rs121918567
PRPH2
0.807 0.080 6 42704609 missense variant C/A;T snv 4.0E-06 6
rs104893769
RHO
0.807 0.160 3 129528783 missense variant C/T snv 7.0E-06 6
rs121912550
IMPDH1
0.827 0.120 7 128398557 missense variant C/T snv 4.0E-06 5
rs1042253
IMPDH1
0.851 0.120 7 128398543 synonymous variant G/A snv 4.0E-06 4
rs200729507
IMPDH1
0.851 0.120 7 128396990 missense variant G/A;C;T snv 7.6E-05; 4.0E-06 4
rs759995866
IMPDH1
0.851 0.120 7 128398478 missense variant G/A snv 4.0E-06 4
rs121912631
NR2E3
0.851 0.080 15 71811530 missense variant G/A;T snv 4
rs104894459
NRL
0.882 0.080 14 24082701 missense variant A/T snv 4
rs137852534
PGK1
0.851 0.120 X 78123196 missense variant T/C snv 1.1E-05 4
rs104893779
RHO
0.851 0.080 3 129532288 missense variant G/A;T snv 4.0E-06 4
rs527236100
RHO
0.851 0.080 3 129532282 missense variant G/A snv 4
rs267607077
SNRNP200
0.882 0.080 2 96287968 missense variant G/A snv 4.0E-06 4
rs121912552
IMPDH1
0.882 0.080 7 128398562 missense variant C/G snv 3
rs397514516
NRL
0.882 0.080 14 24082562 missense variant A/G snv 4.0E-06 3
rs121434241
PRPF3
0.882 0.080 1 150344216 missense variant C/T snv 3
rs119475042
PRPF31
0.882 0.080 19 54123867 missense variant G/A;C snv 4.0E-06 3
rs61755799
PRPH2
0.882 0.160 6 42704560 missense variant G/T snv 3
rs61755805
PRPH2
0.882 0.080 6 42704547 missense variant G/A snv 3
rs61755806
PRPH2
0.882 0.080 6 42704546 missense variant G/A snv 4.0E-06 7.0E-06 3
rs104893773
RHO
0.882 0.080 3 129529049 missense variant G/A;T snv 1.6E-05 3
rs104893781
RHO
0.882 0.080 3 129532636 missense variant C/T snv 3