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rs878853369

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853369(G;T)
Make rs878853369(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197477817
GeneCRB1
is asnp
is mentioned by
dbSNPrs878853369
ebirs878853369
HLIrs878853369
Exacrs878853369
Varsomers878853369
Maprs878853369
PheGenIrs878853369
hapmaprs878853369
1000 genomesrs878853369
hgdprs878853369
ensemblrs878853369
gopubmedrs878853369
geneviewrs878853369
scholarrs878853369
googlers878853369
pharmgkbrs878853369
gwascentralrs878853369
openSNPrs878853369
23andMers878853369
23andMe allrs878853369
SNP Nexus

SNPshotrs878853369
SNPdbers878853369
MSV3drs878853369
GWAS Ctlgrs878853369
Max Magnitude0
ClinVar
Risk rs878853369(T;T)
Alt rs878853369(T;T)
Reference rs878853369(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CRB1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000001.10:g.197446947G>T
CLNSRC
CLNACC RCV000225605.1,