Variant (rsID / SNP)

rs6809699

rs6809699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RY12. Location: chromosome 3, position 151,056,598. Clinical significance in the table: Benign.

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Reference-table entries

P2RY12Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:151056598
Cytoband: 3q25.1
HGVS: NM_022788.5(P2RY12):c.36T>G (p.Gly12=)
Allele change: Silent

Associated conditions / phenotypes

Platelet-type bleeding disorder 8

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.