Variant (rsID / SNP)

rs3751144

rs3751144 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RX7. Location: chromosome 12, position 121,622,239. The table records no clinical significance for this variant.

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Reference-table entries

P2RX7Not classified

Variant type: synonymous_variant
Chromosome / position: 12:121622239
HGVS: NM_002562.6,c.1422C>T,p.Pro474Pro
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.