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Variant (rsID / SNP)

rs117939637

OR51F1

rs117939637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51F1. Location: chromosome 11, position 4,790,890. The table records no clinical significance for this variant.

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Reference-table entries

OR51F1Not classified
Variant type
synonymous_variant
Chromosome / position
11:4790890
HGVS
NM_001004752.2,c.279C>T,p.Ile93Ile
Allele change
Synonymous_I86I

Public references

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