Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7107539

OR8D1

rs7107539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8D1. Location: chromosome 11, position 124,180,282. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR8D1Not classified
Variant type
missense_variant
Chromosome / position
11:124180282
HGVS
NM_001002917.2,c.381T>G,p.Cys127Trp
Allele change
Missense_C127W

Public references

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