Variant (rsID / SNP)

rs3802719

rs3802719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,270,982. 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: 10:73270982
Cytoband: 10q22.1
HGVS: NM_022124.6(CDH23):c.429+13G>A
Allele change: Silent

Associated conditions / phenotypes

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

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.