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rs397517346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517346(A;A)
Make rs397517346(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71789043
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517346
ebirs397517346
HLIrs397517346
Exacrs397517346
Varsomers397517346
Maprs397517346
PheGenIrs397517346
hapmaprs397517346
1000 genomesrs397517346
hgdprs397517346
ensemblrs397517346
gopubmedrs397517346
geneviewrs397517346
scholarrs397517346
googlers397517346
pharmgkbrs397517346
gwascentralrs397517346
openSNPrs397517346
23andMers397517346
23andMe allrs397517346
SNP Nexus

SNPshotrs397517346
SNPdbers397517346
MSV3drs397517346
GWAS Ctlgrs397517346
Max Magnitude0
ClinVar
Risk rs397517346(A;A)
Alt rs397517346(A;A)
Reference rs397517346(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MIR7152 CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73548800G>A
CLNSRC ClinVar
CLNACC RCV000039230.2,