Variant (rsID / SNP)

rs11114486

rs11114486 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRQ. Location: chromosome 12, position 80,899,901. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PTPRQNot classified

Variant type: missense_variant
Chromosome / position: 12:80899901
HGVS: NM_001145026.2,c.1915C>A,p.Gln639Lys
Allele change: Missense_Q619K

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.