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rs878853361

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853361(C;T)
Make rs878853361(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position88083858
GeneCEP290
is asnp
is mentioned by
dbSNPrs878853361
ebirs878853361
HLIrs878853361
Exacrs878853361
Varsomers878853361
Maprs878853361
PheGenIrs878853361
hapmaprs878853361
1000 genomesrs878853361
hgdprs878853361
ensemblrs878853361
gopubmedrs878853361
geneviewrs878853361
scholarrs878853361
googlers878853361
pharmgkbrs878853361
gwascentralrs878853361
openSNPrs878853361
23andMers878853361
23andMe allrs878853361
SNP Nexus

SNPshotrs878853361
SNPdbers878853361
MSV3drs878853361
GWAS Ctlgrs878853361
Max Magnitude0
ClinVar
Risk rs878853361(T;T)
Alt rs878853361(T;T)
Reference rs878853361(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CEP290
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000012.11:g.88477635G>A
CLNSRC
CLNACC RCV000225618.1,