Variant (rsID / SNP)

rs145868749

rs145868749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH23. Location: chromosome 10, position 73,552,960. Clinical significance in the table: Likely benign.

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Reference-table entries

CDH23Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:73552960
Cytoband: 10q22.1
HGVS: NM_022124.6(CDH23):c.6275C>T (p.Thr2092Ile)
Allele change: Missense_T2092I

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.