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rs397517354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517354(C;C)
Make rs397517354(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71805854
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517354
ebirs397517354
HLIrs397517354
Exacrs397517354
Varsomers397517354
Maprs397517354
PheGenIrs397517354
hapmaprs397517354
1000 genomesrs397517354
hgdprs397517354
ensemblrs397517354
gopubmedrs397517354
geneviewrs397517354
scholarrs397517354
googlers397517354
pharmgkbrs397517354
gwascentralrs397517354
openSNPrs397517354
23andMers397517354
23andMe allrs397517354
SNP Nexus

SNPshotrs397517354
SNPdbers397517354
MSV3drs397517354
GWAS Ctlgrs397517354
Max Magnitude0
ClinVar
Risk rs397517354(C;C)
Alt rs397517354(C;C)
Reference rs397517354(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73565611G>C
CLNSRC ClinVar
CLNACC RCV000039277.2,