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Variant (rsID / SNP)

rs6591324

OR8U3

rs6591324 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8U3. Location: chromosome 11, position 56,185,345. The table records no clinical significance for this variant.

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Reference-table entries

OR8U3Not classified
Variant type
missense_variant
Chromosome / position
11:56185345
HGVS
NM_001004744.1,c.364T>C,p.Cys122Arg
Allele change
Missense_C122R

Public references

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