Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893782
RHO
0.882 0.080 3 129532340 missense variant T/G snv 3
rs104893786
RHO
0.882 0.080 3 129528777 missense variant A/G snv 3
rs104893787
RHO
0.882 0.080 3 129529062 missense variant G/A snv 3
rs104893797
RHO
0.882 0.080 3 129528800 missense variant C/G snv 3
rs28933394
RHO
0.882 0.080 3 129528906 missense variant C/G;T snv 9.1E-05 3
rs775557680
RHO
0.882 0.080 3 129532261 missense variant G/A;C snv 8.0E-06 3
rs104894082
RP1
0.882 0.080 8 54625911 stop gained C/T snv 3
rs527236114
SNRNP200
0.882 0.080 2 96293085 missense variant C/A snv 3
rs745455593
IMPDH1
0.925 0.080 7 128400412 missense variant C/T snv 8.0E-06 2.8E-05 2
rs137853114
KLHL7
0.925 0.080 7 23140783 missense variant G/A snv 2
rs1223029749
NR2E3
0.925 0.080 15 71812102 missense variant C/G snv 6.2E-06 7.0E-06 2
rs119475043
PRPF31
0.925 0.080 19 54123802 missense variant C/A;T snv 2
rs61755804
PRPH2
0.925 0.080 6 42704552 missense variant C/G;T snv 2
rs61755816
PRPH2
0.925 0.080 6 42704461 missense variant G/C;T snv 2
rs104893778
RHO
0.925 0.080 3 129533701 stop gained C/T snv 2
rs104893788
RHO
0.925 0.080 3 129529074 missense variant G/A;C snv 4.0E-06 2
rs1422016730
RHO
0.925 0.080 3 129532366 missense variant A/T snv 4.0E-06 2
rs29001653
RHO
0.925 0.080 3 129532722 missense variant A/G snv 2
rs779665096
RHO
0.925 0.080 3 129532731 missense variant G/A;T snv 2.0E-05; 2.3E-04 2
rs121434238
RILP ; PRPF8
0.925 0.080 17 1650881 missense variant C/T snv 2
rs180729424
RP1
0.925 0.080 8 54621481 missense variant T/C;G snv 9.6E-05 2
rs1040241545
C1QTNF5 ; MFRP
1.000 0.080 11 119340235 missense variant G/A;C snv 1
rs549896105
COL6A6
1.000 0.080 3 130563310 missense variant G/A;C;T snv 6.4E-05; 4.0E-06; 8.0E-06 1
rs61748437
CRX
1.000 0.080 19 47836308 missense variant G/A snv 1.6E-05 2.1E-05 1
rs1472664284
ERG
1.000 0.080 21 38423475 missense variant A/G snv 4.0E-06 1