Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853347

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853347(-;-)
Make rs878853347(-;C)
Make rs878853347(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position84196623
GeneCDHR1
is asnp
is mentioned by
dbSNPrs878853347
ebirs878853347
HLIrs878853347
Exacrs878853347
Varsomers878853347
Maprs878853347
PheGenIrs878853347
hapmaprs878853347
1000 genomesrs878853347
hgdprs878853347
ensemblrs878853347
gopubmedrs878853347
geneviewrs878853347
scholarrs878853347
googlers878853347
pharmgkbrs878853347
gwascentralrs878853347
openSNPrs878853347
23andMers878853347
23andMe allrs878853347
SNP Nexus

SNPshotrs878853347
SNPdbers878853347
MSV3drs878853347
GWAS Ctlgrs878853347
Max Magnitude0
ClinVar
Risk rs878853347(C;C)
Alt rs878853347(C;C)
Reference rs878853347(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CDHR1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000010.10:g.85956379dupC
CLNSRC
CLNACC RCV000225405.1,