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rs527236059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236059(A;G)
Make rs527236059(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position47937505
GeneCNGA1, LOC101927157
is asnp
is mentioned by
dbSNPrs527236059
ebirs527236059
HLIrs527236059
Exacrs527236059
Varsomers527236059
Maprs527236059
PheGenIrs527236059
hapmaprs527236059
1000 genomesrs527236059
hgdprs527236059
ensemblrs527236059
gopubmedrs527236059
geneviewrs527236059
scholarrs527236059
googlers527236059
pharmgkbrs527236059
gwascentralrs527236059
openSNPrs527236059
23andMers527236059
23andMe allrs527236059
SNP Nexus

SNPshotrs527236059
SNPdbers527236059
MSV3drs527236059
GWAS Ctlgrs527236059
Max Magnitude0
ClinVar
Risk rs527236059(G;G)
Alt rs527236059(G;G)
Reference rs527236059(A;A)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene CNGA1 LOC101927157
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000004.11:g.47939522T>C
CLNSRC ClinVar
CLNACC RCV000132618.1,