Variant (rsID / SNP)
rs61753164
rs61753164 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RS1. Clinical significance in the table: Likely pathogenic.
Reference-table entries
RS1Likely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- single nucleotide variant
- Cytoband
- Xp22.13
- HGVS
- NM_000330.4(RS1):c.460C>T (p.Gln154Ter)
- Allele change
- Silent
Associated conditions / phenotypes
Retinal dystrophy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.