Variant (rsID / SNP)
rs3890182
rs3890182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA1. Location: chromosome 9, position 107,647,655. Clinical significance in the table: Benign.
Reference-table entries
ABCA1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:107647655
- Cytoband
- 9q31.1
- HGVS
- NM_005502.4(ABCA1):c.161-806C>T
- Allele change
- Silent
Associated conditions / phenotypes
ABCA1 polymorphism
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.