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rs527236097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236097(A;A)
Make rs527236097(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position42721925
GenePRPH2
is asnp
is mentioned by
dbSNPrs527236097
ebirs527236097
HLIrs527236097
Exacrs527236097
Varsomers527236097
Maprs527236097
PheGenIrs527236097
hapmaprs527236097
1000 genomesrs527236097
hgdprs527236097
ensemblrs527236097
gopubmedrs527236097
geneviewrs527236097
scholarrs527236097
googlers527236097
pharmgkbrs527236097
gwascentralrs527236097
openSNPrs527236097
23andMers527236097
23andMe allrs527236097
SNP Nexus

SNPshotrs527236097
SNPdbers527236097
MSV3drs527236097
GWAS Ctlgrs527236097
Max Magnitude0
ClinVar
Risk rs527236097(A;A)
Alt rs527236097(A;A)
Reference rs527236097(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRPH2
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000006.11:g.42689663C>T
CLNSRC ClinVar
CLNACC RCV000132578.1,