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Variant (rsID / SNP)

rs7767176

OR2B6

rs7767176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2B6. Location: chromosome 6, position 27,925,367. The table records no clinical significance for this variant.

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Reference-table entries

OR2B6Not classified
Variant type
missense_variant
Chromosome / position
6:27925367
HGVS
NM_012367.1,c.349G>A,p.Val117Ile
Allele change
Missense_V117I

Public references

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