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rs397517353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517353(A;A)
Make rs397517353(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71803324
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517353
ebirs397517353
HLIrs397517353
Exacrs397517353
Varsomers397517353
Maprs397517353
PheGenIrs397517353
hapmaprs397517353
1000 genomesrs397517353
hgdprs397517353
ensemblrs397517353
gopubmedrs397517353
geneviewrs397517353
scholarrs397517353
googlers397517353
pharmgkbrs397517353
gwascentralrs397517353
openSNPrs397517353
23andMers397517353
23andMe allrs397517353
SNP Nexus

SNPshotrs397517353
SNPdbers397517353
MSV3drs397517353
GWAS Ctlgrs397517353
Max Magnitude0
ClinVar
Risk rs397517353(A;A)
Alt rs397517353(A;A)
Reference rs397517353(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73563081G>A
CLNSRC ClinVar
CLNACC RCV000039275.2,