Variant (rsID / SNP)

rs2546423

rs2546423 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2V2. Location: chromosome 5, position 180,582,604. The table records no clinical significance for this variant.

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Reference-table entries

OR2V2Not classified

Variant type: missense_variant
Chromosome / position: 5:180582604
HGVS: NM_206880.2,c.662A>G,p.His221Arg
Allele change: Missense_H221R

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.