Variant (rsID / SNP)

rs9380122

rs9380122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR12D3, OR5V1. Location: chromosome 6, position 29,342,236. The table records no clinical significance for this variant.

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Reference-table entries

OR12D3Not classified

Variant type: missense_variant
Chromosome / position: 6:29342236
HGVS: NM_030959.3,c.829T>C,p.Tyr277His
Allele change: Missense_Y277H

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.