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rs878853366

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853366(-;-)
Make rs878853366(-;A)
Make rs878853366(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197344435
GeneCRB1
is asnp
is mentioned by
dbSNPrs878853366
ebirs878853366
HLIrs878853366
Exacrs878853366
Varsomers878853366
Maprs878853366
PheGenIrs878853366
hapmaprs878853366
1000 genomesrs878853366
hgdprs878853366
ensemblrs878853366
gopubmedrs878853366
geneviewrs878853366
scholarrs878853366
googlers878853366
pharmgkbrs878853366
gwascentralrs878853366
openSNPrs878853366
23andMers878853366
23andMe allrs878853366
SNP Nexus

SNPshotrs878853366
SNPdbers878853366
MSV3drs878853366
GWAS Ctlgrs878853366
Max Magnitude0
ClinVar
Risk rs878853366(A;A)
Alt rs878853366(A;A)
Reference rs878853366(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CRB1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000001.10:g.197313565dupA
CLNSRC
CLNACC RCV000225488.1,