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rs527236060

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236060(C;C)
Make rs527236060(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position57964482
GeneCNGB1
is asnp
is mentioned by
dbSNPrs527236060
ebirs527236060
HLIrs527236060
Exacrs527236060
Varsomers527236060
Maprs527236060
PheGenIrs527236060
hapmaprs527236060
1000 genomesrs527236060
hgdprs527236060
ensemblrs527236060
gopubmedrs527236060
geneviewrs527236060
scholarrs527236060
googlers527236060
pharmgkbrs527236060
gwascentralrs527236060
openSNPrs527236060
23andMers527236060
23andMe allrs527236060
SNP Nexus

SNPshotrs527236060
SNPdbers527236060
MSV3drs527236060
GWAS Ctlgrs527236060
Max Magnitude0
ClinVar
Risk rs527236060(A,C;A,C)
Alt rs527236060(A,C;A,C)
Reference rs527236060(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene CNGB1
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000016.9:g.57998386C>G
CLNSRC ClinVar
CLNACC RCV000132646.1,