Variant (rsID / SNP)
rs2305795
rs2305795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RY11. Location: chromosome 19, position 10,226,052. Clinical significance in the table: association.
Reference-table entries
P2RY11Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:10226052
- Cytoband
- 19p13.2
- HGVS
- NM_003755.5(EIF3G):c.947+103C>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.