Variant (rsID / SNP)

rs2282316

rs2282316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6F1. Location: chromosome 1, position 247,875,415. The table records no clinical significance for this variant.

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Reference-table entries

OR6F1Not classified

Variant type: missense_variant
Chromosome / position: 1:247875415
HGVS: NM_001005286.2,c.643T>C,p.Phe215Leu
Allele change: Missense_F215L

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.