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rs121908355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908355(A;A)
Make rs121908355(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71615573
GeneCDH23
is asnp
is mentioned by
dbSNPrs121908355
ebirs121908355
HLIrs121908355
Exacrs121908355
Varsomers121908355
Maprs121908355
PheGenIrs121908355
hapmaprs121908355
1000 genomesrs121908355
hgdprs121908355
ensemblrs121908355
gopubmedrs121908355
geneviewrs121908355
scholarrs121908355
googlers121908355
pharmgkbrs121908355
gwascentralrs121908355
openSNPrs121908355
23andMers121908355
23andMe allrs121908355
SNP Nexus

SNPshotrs121908355
SNPdbers121908355
MSV3drs121908355
GWAS Ctlgrs121908355
Max Magnitude0
OMIM605516
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121908355(A;A)
Alt rs121908355(A;A)
Reference rs121908355(G;G)
Significance Pathogenic
Disease Deafness not provided
Variation info
Gene CDH23
CLNDBN Deafness, autosomal recessive 12 not provided
Reversed 0
HGVS NC_000010.10:g.73375330G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005212.3, RCV000173892.1,