Variant (rsID / SNP)
rs1551570
rs1551570 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPAN. Location: chromosome 19, position 10,218,030. Clinical significance in the table: association.
Reference-table entries
PPANAssociation
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:10218030
- Cytoband
- 19p13.2
- HGVS
- NM_020230.7(PPAN):c.190-151C>T
- Allele change
- Silent
Associated conditions / phenotypes
Cataplexy and narcolepsy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.