Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs72873928

OR52E2

rs72873928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52E2. Location: chromosome 11, position 5,080,181. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR52E2Not classified
Variant type
missense_variant
Chromosome / position
11:5080181
HGVS
NM_001005164.2,c.677T>C,p.Val226Ala
Allele change
Missense_V226A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.