Variant (rsID / SNP)
rs890
rs890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIN2B. Location: chromosome 12, position 13,715,308. Clinical significance in the table: Benign.
Reference-table entries
GRIN2BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:13715308
- Cytoband
- 12p13.1
- HGVS
- NM_000834.5(GRIN2B):c.*409T>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.