Variant (rsID / SNP)
rs1884302
rs1884302 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BMP2. Location: chromosome 20, position 7,106,289. Clinical significance in the table: risk factor.
Reference-table entries
BMP2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:7106289
- Cytoband
- 20p12.3
- HGVS
- NC_000020.11:g.7125642T>C
Associated conditions / phenotypes
Craniosynostosis 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.