Variant (rsID / SNP)
rs10769378
rs10769378 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR56A3. Location: chromosome 11, position 5,969,185. The table records no clinical significance for this variant.
Reference-table entries
OR56A3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:5969185
- HGVS
- NM_001003443.3,c.609A>G,p.Gln203Gln
- Allele change
- Synonymous_Q203Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.