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Variant (rsID / SNP)

rs55842922

CLRN1

rs55842922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLRN1. Location: chromosome 3, position 150,690,784. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CLRN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:150690784
Cytoband
3q25.1
HGVS
NM_001195794.1(CLRN1):c.-289G>A
Allele change
Silent

Associated conditions / phenotypes

Usher syndrome type 3

Public references

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