Variant (rsID / SNP)

rs12048482

rs12048482 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10J1. Location: chromosome 1, position 159,409,857. The table records no clinical significance for this variant.

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Reference-table entries

OR10J1Not classified

Variant type: missense_variant
Chromosome / position: 1:159409857
HGVS: NM_001363557.2,c.276A>G,p.Ile92Met
Allele change: Missense_I92M

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.