Variant (rsID / SNP)
rs886042270
rs886042270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPC1. Location: chromosome 18, position 21,124,951. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
NPC1Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 18:21124951
- Cytoband
- 18q11.2
- HGVS
- NM_000271.5(NPC1):c.1920del (p.His641fs)
Associated conditions / phenotypes
Niemann-Pick disease, type C1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.