Variant (rsID / SNP)

rs6664332

rs6664332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2AK2, OR2L13. Location: chromosome 1, position 248,128,929. The table records no clinical significance for this variant.

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Reference-table entries

OR2AK2Not classified

Variant type: missense_variant
Chromosome / position: 1:248128929
HGVS: NM_001004491.2,c.251G>A,p.Ser84Asn
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.