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Variant (rsID / SNP)

rs35771565

OR2W1

rs35771565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2W1. Location: chromosome 6, position 29,012,067. The table records no clinical significance for this variant.

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Reference-table entries

OR2W1Not classified
Variant type
missense_variant
Chromosome / position
6:29012067
HGVS
NM_030903.3,c.886G>A,p.Asp296Asn
Allele change
Silent

Public references

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