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rs527236100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236100(A;A)
Make rs527236100(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position129532282
GeneRHO
is asnp
is mentioned by
dbSNPrs527236100
ebirs527236100
HLIrs527236100
Exacrs527236100
Varsomers527236100
Maprs527236100
PheGenIrs527236100
hapmaprs527236100
1000 genomesrs527236100
hgdprs527236100
ensemblrs527236100
gopubmedrs527236100
geneviewrs527236100
scholarrs527236100
googlers527236100
pharmgkbrs527236100
gwascentralrs527236100
openSNPrs527236100
23andMers527236100
23andMe allrs527236100
SNP Nexus

SNPshotrs527236100
SNPdbers527236100
MSV3drs527236100
GWAS Ctlgrs527236100
Max Magnitude0
ClinVar
Risk rs527236100(A;A)
Alt rs527236100(A;A)
Reference rs527236100(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000003.11:g.129251125G>A
CLNSRC ClinVar
CLNACC RCV000132600.1,