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Variant (rsID / SNP)

rs17127947

OR8D4

rs17127947 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8D4. Location: chromosome 11, position 123,777,302. The table records no clinical significance for this variant.

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Reference-table entries

OR8D4Not classified
Variant type
missense_variant
Chromosome / position
11:123777302
HGVS
NM_001005197.2,c.164T>G,p.Leu55Arg
Allele change
Missense_L55R

Public references

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