Variant (rsID / SNP)

rs7963963

rs7963963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRQ. Location: chromosome 12, position 81,007,527. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PTPRQBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:81007527
Cytoband: 12q21.31
HGVS: NM_001145026.2(PTPRQ):c.5075T>C (p.Ile1692Thr)
Allele change: Missense_I1520T

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.