Variant (rsID / SNP)

rs4883543

rs4883543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RX2, POLE. Location: chromosome 12, position 133,202,004. The table records no clinical significance for this variant.

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Reference-table entries

P2RX2Not classified

Variant type: downstream_gene_variant
Chromosome / position: 12:133202004
HGVS: NM_170683.4,c.*3446C>T
Allele change: Silent

Associated conditions / phenotypes

Oral Cancer|Lip and Oral Cavity Cancer

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.