Gene: RHO ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104893786
rs104893786
RHO
3 0.882 0.080 3 129528777 missense variant A/G snv 0.710 1.000 1 1998 1998
dbSNP: rs104893769
rs104893769
RHO
6 0.807 0.160 3 129528783 missense variant C/T snv 7.0E-06 0.750 1.000 6 2014 2019
dbSNP: rs200946638
rs200946638
RHO
2 0.925 0.080 3 129528786 missense variant G/A;C snv 8.0E-05; 8.0E-06 0.710 1.000 1 2019 2019
dbSNP: rs104893768
rs104893768
RHO
11 0.807 0.080 3 129528801 missense variant C/A snv 0.100 0.950 20 1992 2019
dbSNP: rs1553780837
rs1553780837
RHO
1 1.000 0.080 3 129528816 missense variant A/G snv 0.700 0
dbSNP: rs538820015
rs538820015
RHO
1 1.000 0.080 3 129528857 missense variant G/A snv 1.6E-05 7.0E-06 0.020 1.000 2 2007 2011
dbSNP: rs774336493
rs774336493
RHO
2 0.925 0.080 3 129528864 missense variant T/C snv 4.0E-06 1.4E-05 0.010 1.000 1 1994 1994
dbSNP: rs149079952
rs149079952
RHO
1 1.000 0.080 3 129528885 missense variant G/C snv 8.0E-04 2.9E-03 0.010 1.000 1 2017 2017
dbSNP: rs28933395
rs28933395
RHO
2 0.925 0.080 3 129528891 missense variant C/G snv 0.700 1.000 1 1992 1992
dbSNP: rs28933394
rs28933394
RHO
3 0.882 0.080 3 129528906 missense variant C/G;T snv 9.1E-05 0.010 1.000 1 2015 2015
dbSNP: rs527236101
rs527236101
RHO
1 1.000 0.080 3 129528913 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs104893772
rs104893772
RHO
2 0.925 0.080 3 129528999 missense variant G/A;C snv 0.710 1.000 1 2011 2011
dbSNP: rs104893790
rs104893790
RHO
4 0.851 0.080 3 129529002 missense variant G/A snv 0.010 1.000 1 2011 2011
dbSNP: rs104893773
rs104893773
RHO
3 0.882 0.080 3 129529049 missense variant G/A;T snv 1.6E-05 0.720 1.000 3 1999 2019
dbSNP: rs104893787
rs104893787
RHO
3 0.882 0.080 3 129529062 missense variant G/A snv 0.010 1.000 1 1999 1999
dbSNP: rs762059468
rs762059468
RHO
1 1.000 0.080 3 129530879 missense variant A/G snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs104893775
rs104893775
RHO
7 0.807 0.160 3 129530917 missense variant C/T snv 0.730 1.000 4 2006 2019
dbSNP: rs104893774
rs104893774
RHO
2 0.925 0.080 3 129530918 missense variant G/A;T snv 8.0E-06 0.020 1.000 2 2004 2006
dbSNP: rs886041233
rs886041233
RHO
1 1.000 0.080 3 129530918 missense variant GG/TT mnv 0.020 1.000 2 2004 2006
dbSNP: rs200248198
rs200248198
RHO
2 0.925 0.080 3 129530922 stop gained C/A;T snv 6.8E-05 0.010 1.000 1 2016 2016
dbSNP: rs104893791
rs104893791
RHO
4 0.851 0.080 3 129530962 missense variant G/A;C snv 4.8E-05; 1.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs104893793
rs104893793
RHO
4 0.851 0.080 3 129531005 missense variant C/A;T snv 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs1553781176
rs1553781176
RHO
2 0.925 0.080 3 129531023 missense variant C/G snv 0.700 1.000 1 2001 2001
dbSNP: rs104893794
rs104893794
RHO
2 0.925 0.080 3 129531025 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs527236103
rs527236103
RHO
1 1.000 0.080 3 129531034 missense variant G/A snv 1.2E-05 0.700 0