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rs121908351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908351(A;A)
Make rs121908351(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71732292
GeneCDH23, C10orf105
is asnp
is mentioned by
dbSNPrs121908351
ebirs121908351
HLIrs121908351
Exacrs121908351
Varsomers121908351
Maprs121908351
PheGenIrs121908351
hapmaprs121908351
1000 genomesrs121908351
hgdprs121908351
ensemblrs121908351
gopubmedrs121908351
geneviewrs121908351
scholarrs121908351
googlers121908351
pharmgkbrs121908351
gwascentralrs121908351
openSNPrs121908351
23andMers121908351
23andMe allrs121908351
SNP Nexus

SNPshotrs121908351
SNPdbers121908351
MSV3drs121908351
GWAS Ctlgrs121908351
Max Magnitude0
OMIM605516
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908351(A;A)
Alt rs121908351(A;A)
Reference rs121908351(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene C10orf105 CDH23
CLNDBN Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73492049G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005205.3,