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rs527236090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236090(C;C)
Make rs527236090(C;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position655939
GenePDE6B, RP11-1191J2.2
is asnp
is mentioned by
dbSNPrs527236090
ebirs527236090
HLIrs527236090
Exacrs527236090
Varsomers527236090
Maprs527236090
PheGenIrs527236090
hapmaprs527236090
1000 genomesrs527236090
hgdprs527236090
ensemblrs527236090
gopubmedrs527236090
geneviewrs527236090
scholarrs527236090
googlers527236090
pharmgkbrs527236090
gwascentralrs527236090
openSNPrs527236090
23andMers527236090
23andMe allrs527236090
SNP Nexus

SNPshotrs527236090
SNPdbers527236090
MSV3drs527236090
GWAS Ctlgrs527236090
Max Magnitude0
ClinVar
Risk rs527236090(C;C)
Alt rs527236090(C;C)
Reference rs527236090(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PDE6B RP11-1191J2.2
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.649728G>C
CLNSRC ClinVar
CLNACC RCV000132577.1,