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Variant (rsID / SNP)

rs55966714

WHRN

rs55966714 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WHRN. Location: chromosome 9, position 117,166,272. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WHRNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:117166272
Cytoband
9q32
HGVS
NM_015404.4(WHRN):c.2322C>T (p.Ser774=)
Allele change
Synonymous_S774S

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D

Public references

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