Variant (rsID / SNP)
rs1014531
rs1014531 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIN2A. Location: chromosome 16, position 9,855,794. Clinical significance in the table: Benign.
Reference-table entries
GRIN2ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:9855794
- Cytoband
- 16p13.2
- HGVS
- NM_001134407.3(GRIN2A):c.*1212C>T
- Allele change
- Silent
Associated conditions / phenotypes
Landau-Kleffner syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.