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rs397517329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517329(C;T)
Make rs397517329(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71738597
GeneCDH23, C10orf105
is asnp
is mentioned by
dbSNPrs397517329
ebirs397517329
HLIrs397517329
Exacrs397517329
Varsomers397517329
Maprs397517329
PheGenIrs397517329
hapmaprs397517329
1000 genomesrs397517329
hgdprs397517329
ensemblrs397517329
gopubmedrs397517329
geneviewrs397517329
scholarrs397517329
googlers397517329
pharmgkbrs397517329
gwascentralrs397517329
openSNPrs397517329
23andMers397517329
23andMe allrs397517329
SNP Nexus

SNPshotrs397517329
SNPdbers397517329
MSV3drs397517329
GWAS Ctlgrs397517329
Max Magnitude0
ClinVar
Risk rs397517329(T;T)
Alt rs397517329(T;T)
Reference rs397517329(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene C10orf105 CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73498354C>T
CLNSRC ClinVar
CLNACC RCV000039177.3,