Variant (rsID / SNP)
rs2273073
rs2273073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BMP2. Location: chromosome 20, position 6,750,882. Clinical significance in the table: Benign.
Reference-table entries
BMP2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:6750882
- Cytoband
- 20p12.3
- HGVS
- NM_001200.4(BMP2):c.109T>G (p.Ser37Ala)
- Allele change
- Missense_S37A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.