Variant (rsID / SNP)

rs1466684

rs1466684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RY13. Location: chromosome 3, position 151,046,308. The table records no clinical significance for this variant.

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Reference-table entries

P2RY13Not classified

Variant type: missense_variant
Chromosome / position: 3:151046308
HGVS: NM_176894.3,c.536C>T,p.Thr179Met
Allele change: Silent

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.