Variant (rsID / SNP)
rs61752148
rs61752148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RS1. Clinical significance in the table: Pathogenic.
Reference-table entries
RS1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Microsatellite
- Cytoband
- Xp22.13
- HGVS
- NM_000330.4(RS1):c.375_378del (p.Ile125_Asp126insTer)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.