Variant (rsID / SNP)
rs66866077
rs66866077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BDNF. Location: chromosome 11, position 27,720,937. Clinical significance in the table: Benign.
Reference-table entries
BDNFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:27720937
- Cytoband
- 11p14.1
- HGVS
- NM_001709.5(BDNF):c.-22+774G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.