Variant (rsID / SNP)
rs6265
rs6265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BDNF. Location: chromosome 11, position 27,679,916. Clinical significance in the table: Benign.
Reference-table entries
BDNFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:27679916
- Cytoband
- 11p14.1
- HGVS
- NM_001709.5(BDNF):c.196G>A (p.Val66Met)
- Allele change
- Silent
Associated conditions / phenotypes
Memory impairment, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.