Variant (rsID / SNP)

rs6679056

rs6679056 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10R2. Location: chromosome 1, position 158,450,314. The table records no clinical significance for this variant.

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Reference-table entries

OR10R2Not classified

Variant type: missense_variant
Chromosome / position: 1:158450314
HGVS: NM_001004472.1,c.647A>G,p.Glu216Gly
Allele change: Missense_E216G

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.