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rs878853364

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853364(-;-)
Make rs878853364(-;CTTA)
Make rs878853364(CTTA;CTTA)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197421440
GeneCRB1
is asnp
is mentioned by
dbSNPrs878853364
ebirs878853364
HLIrs878853364
Exacrs878853364
Varsomers878853364
Maprs878853364
PheGenIrs878853364
hapmaprs878853364
1000 genomesrs878853364
hgdprs878853364
ensemblrs878853364
gopubmedrs878853364
geneviewrs878853364
scholarrs878853364
googlers878853364
pharmgkbrs878853364
gwascentralrs878853364
openSNPrs878853364
23andMers878853364
23andMe allrs878853364
SNP Nexus

SNPshotrs878853364
SNPdbers878853364
MSV3drs878853364
GWAS Ctlgrs878853364
Max Magnitude0
ClinVar
Risk rs878853364(CTTA;CTTA)
Alt rs878853364(CTTA;CTTA)
Reference rs878853364(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CRB1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000001.10:g.197390570_197390571insCTTA
CLNSRC
CLNACC RCV000225570.1,