Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs11825515

OR10G8

rs11825515 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10G8. Location: chromosome 11, position 123,901,175. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR10G8Not classified
Variant type
synonymous_variant
Chromosome / position
11:123901175
HGVS
NM_001004464.2,c.846C>A,p.Leu282Leu
Allele change
Synonymous_L282L

Public references

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