Variant (rsID / SNP)

rs2731073

rs2731073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8S1. Location: chromosome 12, position 48,919,556. The table records no clinical significance for this variant.

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Reference-table entries

OR8S1Not classified

Variant type: missense_variant
Chromosome / position: 12:48919556
HGVS: NM_001390849.1,c.142A>G,p.Met48Val
Allele change: Missense_M48V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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