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Variant (rsID / SNP)

rs150894638

CDH23

rs150894638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,490,213. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CDH23Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:73490213
Cytoband
10q22.1
HGVS
NM_022124.6(CDH23):c.3580-13C>T
Allele change
Silent

Associated conditions / phenotypes

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

Public references

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