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Variant (rsID / SNP)

rs28568406

OR6K3

rs28568406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6K3. Location: chromosome 1, position 158,687,163. The table records no clinical significance for this variant.

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Reference-table entries

OR6K3Not classified
Variant type
missense_variant
Chromosome / position
1:158687163
HGVS
NM_001005327.3,c.743C>T,p.Pro248Leu
Allele change
Missense_P248L

Public references

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