Variant (rsID / SNP)
rs111033264
rs111033264 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USH2A. Location: chromosome 1, position 215,956,104. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
USH2APathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:215956104
- Cytoband
- 1q41
- HGVS
- NM_206933.4(USH2A):c.10561T>C (p.Trp3521Arg)
- Allele change
- Missense_W3521R
Associated conditions / phenotypes
Usher syndrome type 2A|Usher syndrome|Retinitis pigmentosa 39|Usher syndrome type 2A|Rare genetic deafness|Retinal dystrophy|Retinitis pigmentosa 39|See cases
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.