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rs397517326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517326(C;T)
Make rs397517326(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position71730517
GeneCDH23, C10orf105
is asnp
is mentioned by
dbSNPrs397517326
ClinGenrs397517326
ebirs397517326
HLIrs397517326
Exacrs397517326
Varsomers397517326
Maprs397517326
PheGenIrs397517326
hapmaprs397517326
1000 genomesrs397517326
hgdprs397517326
ensemblrs397517326
gopubmedrs397517326
geneviewrs397517326
scholarrs397517326
googlers397517326
pharmgkbrs397517326
gwascentralrs397517326
openSNPrs397517326
23andMers397517326
23andMe allrs397517326
SNP Nexus

SNPshotrs397517326
SNPdbers397517326
MSV3drs397517326
GWAS Ctlgrs397517326
Max Magnitude0
ClinVar
Risk rs397517326(T;T)
Alt rs397517326(T;T)
Reference Rs397517326(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene C10orf105 CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73490274C>T
CLNSRC ClinVar
CLNACC RCV000039160.2,