Variant (rsID / SNP)
rs2277405
rs2277405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC9. Location: chromosome 12, position 22,078,838. Clinical significance in the table: Benign.
Reference-table entries
ABCC9Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:22078838
- Cytoband
- 12p12.1
- HGVS
- NM_020297.4(ABCC9):c.406+38A>C
- Allele change
- Silent
Associated conditions / phenotypes
Hypertrichotic osteochondrodysplasia Cantu type
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.