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rs527236106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236106(A;A)
Make rs527236106(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position54628758
GeneRP1
is asnp
is mentioned by
dbSNPrs527236106
ebirs527236106
HLIrs527236106
Exacrs527236106
Varsomers527236106
Maprs527236106
PheGenIrs527236106
hapmaprs527236106
1000 genomesrs527236106
hgdprs527236106
ensemblrs527236106
gopubmedrs527236106
geneviewrs527236106
scholarrs527236106
googlers527236106
pharmgkbrs527236106
gwascentralrs527236106
openSNPrs527236106
23andMers527236106
23andMe allrs527236106
SNP Nexus

SNPshotrs527236106
SNPdbers527236106
MSV3drs527236106
GWAS Ctlgrs527236106
Max Magnitude0
ClinVar
Risk rs527236106(A;A)
Alt rs527236106(A;A)
Reference rs527236106(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000008.10:g.55541318G>A
CLNSRC ClinVar
CLNACC RCV000132659.1,