Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1905055

OR8K1

rs1905055 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8K1. Location: chromosome 11, position 56,113,516. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR8K1Not classified
Variant type
start_lost
Chromosome / position
11:56113516
HGVS
NM_001002907.1,c.2T>C,p.Met1?
Allele change
Missense_M1T

Public references

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