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rs527236061

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs527236061(-;-)
Make rs527236061(-;A)
Make rs527236061(A;A)
ReferenceGRCh38 38.1/142
Chromosome16
Position57904843
GeneCNGB1
is asnp
is mentioned by
dbSNPrs527236061
ebirs527236061
HLIrs527236061
Exacrs527236061
Varsomers527236061
Maprs527236061
PheGenIrs527236061
hapmaprs527236061
1000 genomesrs527236061
hgdprs527236061
ensemblrs527236061
gopubmedrs527236061
geneviewrs527236061
scholarrs527236061
googlers527236061
pharmgkbrs527236061
gwascentralrs527236061
openSNPrs527236061
23andMers527236061
23andMe allrs527236061
SNP Nexus

SNPshotrs527236061
SNPdbers527236061
MSV3drs527236061
GWAS Ctlgrs527236061
Max Magnitude0
ClinVar
Risk rs527236061(A;A)
Alt rs527236061(A;A)
Reference rs527236061(;)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene CNGB1
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000016.9:g.57938748dupT
CLNSRC ClinVar
CLNACC RCV000132647.1,