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rs527236103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236103(A;A)
Make rs527236103(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position129531034
GeneRHO
is asnp
is mentioned by
dbSNPrs527236103
dbSNP (classic)rs527236103
ClinGenrs527236103
ebirs527236103
HLIrs527236103
Exacrs527236103
Gnomadrs527236103
Varsomers527236103
LitVarrs527236103
Maprs527236103
PheGenIrs527236103
Biobankrs527236103
1000 genomesrs527236103
hgdprs527236103
ensemblrs527236103
geneviewrs527236103
scholarrs527236103
googlers527236103
pharmgkbrs527236103
gwascentralrs527236103
openSNPrs527236103
23andMers527236103
SNPshotrs527236103
SNPdbers527236103
MSV3drs527236103
GWAS Ctlgrs527236103
Max Magnitude0
ClinVar
Risk rs527236103(A;A)
Alt rs527236103(A;A)
Reference Rs527236103(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000003.11:g.129249877G>A
CLNSRC ClinVar
CLNACC RCV000132599.1,