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rs527236098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236098(A;A)
Make rs527236098(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position42721836
GenePRPH2
is asnp
is mentioned by
dbSNPrs527236098
ebirs527236098
HLIrs527236098
Exacrs527236098
Varsomers527236098
Maprs527236098
PheGenIrs527236098
hapmaprs527236098
1000 genomesrs527236098
hgdprs527236098
ensemblrs527236098
gopubmedrs527236098
geneviewrs527236098
scholarrs527236098
googlers527236098
pharmgkbrs527236098
gwascentralrs527236098
openSNPrs527236098
23andMers527236098
23andMe allrs527236098
SNP Nexus

SNPshotrs527236098
SNPdbers527236098
MSV3drs527236098
GWAS Ctlgrs527236098
Max Magnitude0
ClinVar
Risk rs527236098(A;A)
Alt rs527236098(A;A)
Reference rs527236098(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRPH2
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000006.11:g.42689574C>T
CLNSRC ClinVar
CLNACC RCV000132579.1,