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rs397517349

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517349(C;T)
Make rs397517349(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71793542
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517349
ebirs397517349
HLIrs397517349
Exacrs397517349
Varsomers397517349
Maprs397517349
PheGenIrs397517349
hapmaprs397517349
1000 genomesrs397517349
hgdprs397517349
ensemblrs397517349
gopubmedrs397517349
geneviewrs397517349
scholarrs397517349
googlers397517349
pharmgkbrs397517349
gwascentralrs397517349
openSNPrs397517349
23andMers397517349
23andMe allrs397517349
SNP Nexus

SNPshotrs397517349
SNPdbers397517349
MSV3drs397517349
GWAS Ctlgrs397517349
Max Magnitude0
ClinVar
Risk rs397517349(T;T)
Alt rs397517349(T;T)
Reference rs397517349(C;C)
Significance Probable-Pathogenic
Disease not specified not provided Inborn genetic diseases
Variation info
Gene CDH23
CLNDBN not specified not provided Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.73553299C>T
CLNSRC
CLNACC RCV000039250.3, RCV000171176.1, RCV000210550.1,