Variant (rsID / SNP)
rs7432766
rs7432766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,626,928. Clinical significance in the table: Benign.
Reference-table entries
SCN5ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38626928
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.2787+254A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.