Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs79724132

OR4F15

rs79724132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4F15. Location: chromosome 15, position 102,359,203. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR4F15Not classified
Variant type
missense_variant
Chromosome / position
15:102359203
HGVS
NM_001001674.2,c.814G>A,p.Ala272Thr
Allele change
Missense_A272T

Public references

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