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rs527236057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236057(A;A)
Make rs527236057(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position47936861
GeneCNGA1, LOC101927157
is asnp
is mentioned by
dbSNPrs527236057
ebirs527236057
HLIrs527236057
Exacrs527236057
Varsomers527236057
Maprs527236057
PheGenIrs527236057
hapmaprs527236057
1000 genomesrs527236057
hgdprs527236057
ensemblrs527236057
gopubmedrs527236057
geneviewrs527236057
scholarrs527236057
googlers527236057
pharmgkbrs527236057
gwascentralrs527236057
openSNPrs527236057
23andMers527236057
23andMe allrs527236057
SNP Nexus

SNPshotrs527236057
SNPdbers527236057
MSV3drs527236057
GWAS Ctlgrs527236057
Max Magnitude0
ClinVar
Risk rs527236057(A;A)
Alt rs527236057(A;A)
Reference rs527236057(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene CNGA1 LOC101927157
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000004.11:g.47938878C>T
CLNSRC ClinVar
CLNACC RCV000132619.1,