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rs876657718

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657718(A;A)
Make rs876657718(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position625917
GenePDE6B
is asnp
is mentioned by
dbSNPrs876657718
ebirs876657718
HLIrs876657718
Exacrs876657718
Varsomers876657718
Maprs876657718
PheGenIrs876657718
hapmaprs876657718
1000 genomesrs876657718
hgdprs876657718
ensemblrs876657718
gopubmedrs876657718
geneviewrs876657718
scholarrs876657718
googlers876657718
pharmgkbrs876657718
gwascentralrs876657718
openSNPrs876657718
23andMers876657718
23andMe allrs876657718
SNP Nexus

SNPshotrs876657718
SNPdbers876657718
MSV3drs876657718
GWAS Ctlgrs876657718
Max Magnitude0
ClinVar
Risk rs876657718(A;A)
Alt rs876657718(A;A)
Reference rs876657718(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa Retinal dystrophy
Variation info
Gene PDE6B
CLNDBN Retinitis pigmentosa Retinal dystrophy
Reversed 0
HGVS NC_000004.11:g.619706C>A
CLNSRC
CLNACC RCV000220232.1, RCV000225461.1,