Variant (rsID / SNP)
rs397517964
rs397517964 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USH2A. Location: chromosome 1, position 215,960,208. Clinical significance in the table: Pathogenic.
Reference-table entries
USH2APathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 1:215960208
- Cytoband
- 1q41
- HGVS
- NM_206933.4(USH2A):c.10190_10191del (p.Lys3397fs)
Associated conditions / phenotypes
Rare genetic deafness|Retinitis pigmentosa 39
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.