Variant (rsID / SNP)

rs121917885

rs121917885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RY12. Location: chromosome 3, position 151,055,867. Clinical significance in the table: Uncertain significance.

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Reference-table entries

P2RY12Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:151055867
Cytoband: 3q25.1
HGVS: NM_022788.5(P2RY12):c.767G>A (p.Arg256Gln)
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.