Gene: RHO ×
Source: CLINVAR ×
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: rs104893789
rs104893789
RHO
1 0.882 0.080 3 129532711 missense variant C/A snv 0.800 1.000 0 1993 1999
dbSNP: rs104893790
rs104893790
RHO
1 0.851 0.080 3 129529002 missense variant G/A snv 0.800 1.000 0 1993 1999
dbSNP: rs104893796
rs104893796
RHO
1 0.851 0.080 3 129529014 missense variant C/T snv 0.800 1.000 0 1993 1999
dbSNP: rs104893793
rs104893793
RHO
4 0.851 0.080 3 129531005 missense variant C/A;T snv 4.0E-06 0.700 1.000 7 1994 2011
dbSNP: rs104893768
rs104893768
RHO
3 0.807 0.080 3 129528801 missense variant C/A snv 0.700 0