Variant (rsID / SNP)
rs143689400
rs143689400 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLMAP. Location: chromosome 3, position 57,902,766. Clinical significance in the table: Likely benign.
Reference-table entries
SLMAPLikely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:57902766
- Cytoband
- 3p14.3
- HGVS
- NM_001377540.1(SLMAP):c.2272A>T (p.Ser758Cys)
- Allele change
- Missense_S703C
Associated conditions / phenotypes
Brugada syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.