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rs527236062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236062(C;C)
Make rs527236062(C;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position47836335
GeneCRX
is asnp
is mentioned by
dbSNPrs527236062
ebirs527236062
HLIrs527236062
Exacrs527236062
Varsomers527236062
Maprs527236062
PheGenIrs527236062
hapmaprs527236062
1000 genomesrs527236062
hgdprs527236062
ensemblrs527236062
gopubmedrs527236062
geneviewrs527236062
scholarrs527236062
googlers527236062
pharmgkbrs527236062
gwascentralrs527236062
openSNPrs527236062
23andMers527236062
23andMe allrs527236062
SNP Nexus

SNPshotrs527236062
SNPdbers527236062
MSV3drs527236062
GWAS Ctlgrs527236062
Max Magnitude0
ClinVar
Risk rs527236062(C;C)
Alt rs527236062(C;C)
Reference rs527236062(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene CRX
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000019.9:g.48339592G>C
CLNSRC ClinVar
CLNACC RCV000132604.1,