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

rs878853337

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853337(C;G)
Make rs878853337(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71805841
GeneCDH23
is asnp
is mentioned by
dbSNPrs878853337
ebirs878853337
HLIrs878853337
Exacrs878853337
Varsomers878853337
Maprs878853337
PheGenIrs878853337
hapmaprs878853337
1000 genomesrs878853337
hgdprs878853337
ensemblrs878853337
gopubmedrs878853337
geneviewrs878853337
scholarrs878853337
googlers878853337
pharmgkbrs878853337
gwascentralrs878853337
openSNPrs878853337
23andMers878853337
23andMe allrs878853337
SNP Nexus

SNPshotrs878853337
SNPdbers878853337
MSV3drs878853337
GWAS Ctlgrs878853337
Max Magnitude0
ClinVar
Risk rs878853337(G;G)
Alt rs878853337(G;G)
Reference rs878853337(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CDH23
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000010.10:g.73565598C>G
CLNSRC
CLNACC RCV000225547.1,