Variant (rsID / SNP)
rs17277522
rs17277522 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6S1. Location: chromosome 14, position 21,109,141. The table records no clinical significance for this variant.
Reference-table entries
OR6S1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:21109141
- HGVS
- NM_001001968.1,c.710G>A,p.Arg237His
- Allele change
- Missense_R237H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.