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: rs104893783
rs104893783
RHO
2 0.925 0.080 3 129532581 stop gained G/A;T snv 4.0E-06; 2.0E-05 0.010 1.000 1 1993 1993
dbSNP: rs104893787
rs104893787
RHO
3 0.882 0.080 3 129529062 missense variant G/A snv 0.010 1.000 1 1999 1999
dbSNP: rs104893790
rs104893790
RHO
4 0.851 0.080 3 129529002 missense variant G/A snv 0.010 1.000 1 2011 2011
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: rs1236550448
rs1236550448
RHO
1 1.000 0.080 3 129532273 missense variant T/C snv 0.010 1.000 1 2014 2014
dbSNP: rs1422016730
rs1422016730
RHO
2 0.925 0.080 3 129532366 missense variant A/T snv 4.0E-06 0.010 1.000 1 2012 2012
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: 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: 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: rs567288669
rs567288669
RHO
1 1.000 0.080 3 129532345 missense variant G/A snv 1.2E-05 3.5E-05 0.010 1.000 1 2018 2018
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: rs766161322
rs766161322
RHO
2 0.925 0.080 3 129532379 missense variant T/G snv 2.0E-05 0.010 1.000 1 2018 2018
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: rs779665096
rs779665096
RHO
2 0.925 0.080 3 129532731 missense variant G/A;T snv 2.0E-05; 2.3E-04 0.010 1.000 1 2001 2001
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: 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: rs886041233
rs886041233
RHO
1 1.000 0.080 3 129530918 missense variant GG/TT mnv 0.020 1.000 2 2004 2006
dbSNP: rs104893768
rs104893768
RHO
11 0.807 0.080 3 129528801 missense variant C/A snv 0.100 0.950 20 1992 2019
dbSNP: rs104893776
rs104893776
RHO
2 0.925 0.080 3 129532253 missense variant A/G snv 0.700 1.000 1 2019 2019
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: rs28933395
rs28933395
RHO
2 0.925 0.080 3 129528891 missense variant C/G snv 0.700 1.000 1 1992 1992
dbSNP: rs104893794
rs104893794
RHO
2 0.925 0.080 3 129531025 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1553780837
rs1553780837
RHO
1 1.000 0.080 3 129528816 missense variant A/G snv 0.700 0
dbSNP: rs527236100
rs527236100
RHO
4 0.851 0.080 3 129532282 missense variant G/A snv 0.700 0