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Variant (rsID / SNP)

rs188966938

CDH23

rs188966938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,570,263. 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
10:73570263
Cytoband
10q22.1
HGVS
NM_022124.6(CDH23):c.9014C>G (p.Ala3005Gly)
Allele change
Missense_A3005G

Associated conditions / phenotypes

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

Public references

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