Variant (rsID / SNP)
rs2325788
rs2325788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RX1. Location: chromosome 17, position 3,818,830. The table records no clinical significance for this variant.
Reference-table entries
P2RX1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 17:3818830
- HGVS
- NM_002558.4,c.137+553T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.