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rs527236091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236091(A;A)
Make rs527236091(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position660575
GenePDE6B
is asnp
is mentioned by
dbSNPrs527236091
ebirs527236091
HLIrs527236091
Exacrs527236091
Varsomers527236091
Maprs527236091
PheGenIrs527236091
hapmaprs527236091
1000 genomesrs527236091
hgdprs527236091
ensemblrs527236091
gopubmedrs527236091
geneviewrs527236091
scholarrs527236091
googlers527236091
pharmgkbrs527236091
gwascentralrs527236091
openSNPrs527236091
23andMers527236091
23andMe allrs527236091
SNP Nexus

SNPshotrs527236091
SNPdbers527236091
MSV3drs527236091
GWAS Ctlgrs527236091
Max Magnitude0
ClinVar
Risk rs527236091(A;A)
Alt rs527236091(A;A)
Reference rs527236091(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.654364G>A
CLNSRC ClinVar
CLNACC RCV000132574.1,