Variant (rsID / SNP)
rs2391191
rs2391191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAOA, DAOA-AS1. Location: chromosome 13, position 106,119,446. The table records no clinical significance for this variant.
Reference-table entries
DAOANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:106119446
- Cytoband
- 13q33.2
- HGVS
- NM_172370.5(DAOA):c.89G>A (p.Arg30Lys)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.