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rs527236088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236088(A;A)
Make rs527236088(A;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position660603
GenePDE6B
is asnp
is mentioned by
dbSNPrs527236088
ebirs527236088
HLIrs527236088
Exacrs527236088
Varsomers527236088
Maprs527236088
PheGenIrs527236088
hapmaprs527236088
1000 genomesrs527236088
hgdprs527236088
ensemblrs527236088
gopubmedrs527236088
geneviewrs527236088
scholarrs527236088
googlers527236088
pharmgkbrs527236088
gwascentralrs527236088
openSNPrs527236088
23andMers527236088
23andMe allrs527236088
SNP Nexus

SNPshotrs527236088
SNPdbers527236088
MSV3drs527236088
GWAS Ctlgrs527236088
Max Magnitude0
ClinVar
Risk rs527236088(A;A)
Alt rs527236088(A;A)
Reference rs527236088(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.654392T>A
CLNSRC ClinVar
CLNACC RCV000132575.1,