Variant (rsID / SNP)

rs16846663

rs16846663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLRN1. Location: chromosome 3, position 150,658,264. Clinical significance in the table: Benign.

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Reference-table entries

CLRN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:150658264
Cytoband: 3q25.1
HGVS: NM_174878.3(CLRN1):c.433+1105C>T
Allele change: Silent

Associated conditions / phenotypes

Usher syndrome type 3A

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.