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rs397517341

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517341(A;A)
Make rs397517341(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71785101
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517341
ebirs397517341
HLIrs397517341
Exacrs397517341
Varsomers397517341
Maprs397517341
PheGenIrs397517341
hapmaprs397517341
1000 genomesrs397517341
hgdprs397517341
ensemblrs397517341
gopubmedrs397517341
geneviewrs397517341
scholarrs397517341
googlers397517341
pharmgkbrs397517341
gwascentralrs397517341
openSNPrs397517341
23andMers397517341
23andMe allrs397517341
SNP Nexus

SNPshotrs397517341
SNPdbers397517341
MSV3drs397517341
GWAS Ctlgrs397517341
Max Magnitude0
ClinVar
Risk rs397517341(A;A)
Alt rs397517341(A;A)
Reference rs397517341(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73544858G>A
CLNSRC ClinVar
CLNACC RCV000039223.2,