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rs527236096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236096(C;C)
Make rs527236096(C;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position63995027
GenePRPF6
is asnp
is mentioned by
dbSNPrs527236096
ebirs527236096
HLIrs527236096
Exacrs527236096
Varsomers527236096
Maprs527236096
PheGenIrs527236096
hapmaprs527236096
1000 genomesrs527236096
hgdprs527236096
ensemblrs527236096
gopubmedrs527236096
geneviewrs527236096
scholarrs527236096
googlers527236096
pharmgkbrs527236096
gwascentralrs527236096
openSNPrs527236096
23andMers527236096
23andMe allrs527236096
SNP Nexus

SNPshotrs527236096
SNPdbers527236096
MSV3drs527236096
GWAS Ctlgrs527236096
Max Magnitude0
ClinVar
Risk rs527236096(C;C)
Alt rs527236096(C;C)
Reference rs527236096(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRPF6
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000020.10:g.62626380G>C
CLNSRC ClinVar
CLNACC RCV000132667.1,