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rs202052174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202052174(A;A)
Make rs202052174(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71803371
GeneCDH23
is asnp
is mentioned by
dbSNPrs202052174
ebirs202052174
HLIrs202052174
Exacrs202052174
Varsomers202052174
Maprs202052174
PheGenIrs202052174
hapmaprs202052174
1000 genomesrs202052174
hgdprs202052174
ensemblrs202052174
gopubmedrs202052174
geneviewrs202052174
scholarrs202052174
googlers202052174
pharmgkbrs202052174
gwascentralrs202052174
openSNPrs202052174
23andMers202052174
23andMe allrs202052174
SNP Nexus

SNPshotrs202052174
SNPdbers202052174
MSV3drs202052174
GWAS Ctlgrs202052174
Max Magnitude0
ClinVar
Risk rs202052174(A;A)
Alt rs202052174(A;A)
Reference rs202052174(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene CDH23
CLNDBN not specified
Reversed 0
HGVS NC_000010.10:g.73563128G>A
CLNSRC ClinVar
CLNACC RCV000039276.3,