Variant (rsID / SNP)
rs3495
rs3495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCHE. Location: chromosome 3, position 165,490,981. Clinical significance in the table: Benign.
Reference-table entries
BCHEBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:165490981
- Cytoband
- 3q26.1
- HGVS
- NM_000055.4(BCHE):c.*189G>A
- Allele change
- Silent
Associated conditions / phenotypes
Deficiency of butyrylcholinesterase
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.