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Variant (rsID / SNP)

rs7926767

OR8D4

rs7926767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8D4. Location: chromosome 11, position 123,777,536. The table records no clinical significance for this variant.

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Reference-table entries

OR8D4Not classified
Variant type
missense_variant
Chromosome / position
11:123777536
HGVS
NM_001005197.2,c.398G>A,p.Arg133Lys
Allele change
Missense_R133K

Public references

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