Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434241
PRPF3
0.882 0.080 1 150344216 missense variant C/T snv 3
rs41265017
SEMA4A
1.000 0.080 1 156176849 missense variant G/A snv 3.7E-02 3.2E-02 1
rs267607077
SNRNP200
0.882 0.080 2 96287968 missense variant G/A snv 4.0E-06 4
rs527236114
SNRNP200
0.882 0.080 2 96293085 missense variant C/A snv 3
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
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
rs104893769
RHO
0.807 0.160 3 129528783 missense variant C/T snv 7.0E-06 6
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
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
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
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
rs141956356
RHO
1.000 0.080 3 129532380 missense variant T/G snv 4.4E-05 4.2E-05 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