Variant (rsID / SNP)
rs7971073
rs7971073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6C65. Location: chromosome 12, position 55,794,976. The table records no clinical significance for this variant.
Reference-table entries
OR6C65Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:55794976
- HGVS
- NM_001005518.1,c.664A>G,p.Thr222Ala
- Allele change
- Missense_T222A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.