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rs397517342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517342(A;A)
Make rs397517342(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71785100
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517342
ebirs397517342
HLIrs397517342
Exacrs397517342
Varsomers397517342
Maprs397517342
PheGenIrs397517342
hapmaprs397517342
1000 genomesrs397517342
hgdprs397517342
ensemblrs397517342
gopubmedrs397517342
geneviewrs397517342
scholarrs397517342
googlers397517342
pharmgkbrs397517342
gwascentralrs397517342
openSNPrs397517342
23andMers397517342
23andMe allrs397517342
SNP Nexus

SNPshotrs397517342
SNPdbers397517342
MSV3drs397517342
GWAS Ctlgrs397517342
Max Magnitude0
ClinVar
Risk rs397517342(A;A)
Alt rs397517342(A;A)
Reference rs397517342(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73544857G>A
CLNSRC ClinVar
CLNACC RCV000039224.2,