Variant (rsID / SNP)

rs6658227

rs6658227 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2L3, OR2L13. Location: chromosome 1, position 248,224,216. The table records no clinical significance for this variant.

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Reference-table entries

OR2L3Not classified

Variant type: missense_variant
Chromosome / position: 1:248224216
HGVS: NM_001004687.2,c.233C>T,p.Pro78Leu
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.