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rs527236092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236092(C;C)
Make rs527236092(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position76540143
GenePRCD
is asnp
is mentioned by
dbSNPrs527236092
ebirs527236092
HLIrs527236092
Exacrs527236092
Varsomers527236092
Maprs527236092
PheGenIrs527236092
hapmaprs527236092
1000 genomesrs527236092
hgdprs527236092
ensemblrs527236092
gopubmedrs527236092
geneviewrs527236092
scholarrs527236092
googlers527236092
pharmgkbrs527236092
gwascentralrs527236092
openSNPrs527236092
23andMers527236092
23andMe allrs527236092
SNP Nexus

SNPshotrs527236092
SNPdbers527236092
MSV3drs527236092
GWAS Ctlgrs527236092
Max Magnitude0
ClinVar
Risk rs527236092(C;C)
Alt rs527236092(C;C)
Reference rs527236092(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRCD
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000017.10:g.74536225T>C
CLNSRC ClinVar
CLNACC RCV000132616.1,