Variant (rsID / SNP)

rs10823829

rs10823829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,466,709. Clinical significance in the table: Benign.

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Reference-table entries

CDH23Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:73466709
Cytoband: 10q22.1
HGVS: NM_022124.6(CDH23):c.3009T>C (p.Ser1003=)
Allele change: Synonymous_S1003S

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 12|Usher syndrome type 1D|Usher syndrome type 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.