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Variant (rsID / SNP)

rs146273185

WHRN

rs146273185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WHRN. Location: chromosome 9, position 117,241,002. 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
9:117241002
Cytoband
9q32
HGVS
NM_015404.4(WHRN):c.668G>A (p.Arg223His)
Allele change
Missense_R223H

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.