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rs878853371

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853371(C;T)
Make rs878853371(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197434732
GeneCRB1
is asnp
is mentioned by
dbSNPrs878853371
ebirs878853371
HLIrs878853371
Exacrs878853371
Varsomers878853371
Maprs878853371
PheGenIrs878853371
hapmaprs878853371
1000 genomesrs878853371
hgdprs878853371
ensemblrs878853371
gopubmedrs878853371
geneviewrs878853371
scholarrs878853371
googlers878853371
pharmgkbrs878853371
gwascentralrs878853371
openSNPrs878853371
23andMers878853371
23andMe allrs878853371
SNP Nexus

SNPshotrs878853371
SNPdbers878853371
MSV3drs878853371
GWAS Ctlgrs878853371
Max Magnitude0
ClinVar
Risk rs878853371(T;T)
Alt rs878853371(T;T)
Reference rs878853371(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CRB1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000001.10:g.197403862C>T
CLNSRC
CLNACC RCV000225597.1,