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rs397517327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517327(C;T)
Make rs397517327(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71730595
GeneCDH23, C10orf105
is asnp
is mentioned by
dbSNPrs397517327
ebirs397517327
HLIrs397517327
Exacrs397517327
Varsomers397517327
Maprs397517327
PheGenIrs397517327
hapmaprs397517327
1000 genomesrs397517327
hgdprs397517327
ensemblrs397517327
gopubmedrs397517327
geneviewrs397517327
scholarrs397517327
googlers397517327
pharmgkbrs397517327
gwascentralrs397517327
openSNPrs397517327
23andMers397517327
23andMe allrs397517327
SNP Nexus

SNPshotrs397517327
SNPdbers397517327
MSV3drs397517327
GWAS Ctlgrs397517327
Max Magnitude0
ClinVar
Risk rs397517327(T;T)
Alt rs397517327(T;T)
Reference rs397517327(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene C10orf105 CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73490352C>T
CLNSRC ClinVar
CLNACC RCV000039163.2,