Variant (rsID / SNP)

rs6591323

rs6591323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8U3, OR5AL1. Location: chromosome 11, position 56,180,753. The table records no clinical significance for this variant.

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Reference-table entries

OR8U3Not classified

Variant type: downstream_gene_variant
Chromosome / position: 11:56180753
HGVS: NM_001004744.1,c.*3981T>C
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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