Variant (rsID / SNP)
rs6785930
rs6785930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RY12. Location: chromosome 3, position 151,056,616. Clinical significance in the table: Benign.
Reference-table entries
P2RY12Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:151056616
- Cytoband
- 3q25.1
- HGVS
- NM_022788.5(P2RY12):c.18C>T (p.Asn6=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.