Variant (rsID / SNP)
rs114964332
rs114964332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BNC2. Location: chromosome 9, position 16,437,276. Clinical significance in the table: Benign.
Reference-table entries
BNC2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:16437276
- Cytoband
- 9p22.3
- HGVS
- NM_017637.6(BNC2):c.916C>G (p.Pro306Ala)
- Allele change
- Missense_P306A
Associated conditions / phenotypes
Hypotension
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.