Variant (rsID / SNP)

rs143664462

rs143664462 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RX2. Location: chromosome 12, position 133,196,062. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

P2RX2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:133196062
Cytoband: 12q24.33
HGVS: NM_170682.4(P2RX2):c.211G>A (p.Glu71Lys)
Allele change: Missense_E71K

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.