Variant (rsID / SNP)

rs75585377

rs75585377 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P2RX2. Location: chromosome 12, position 133,196,037. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

P2RX2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:133196037
Cytoband: 12q24.33
HGVS: NM_170682.4(P2RX2):c.186C>T (p.Ile62=)
Allele change: Synonymous_I62I

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.