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Variant (rsID / SNP)

rs7903502

CDH23

rs7903502 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,377,163. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDH23Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:73377163
Cytoband
10q22.1
HGVS
NM_022124.6(CDH23):c.1134+13A>G
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.