Variant (rsID / SNP)
rs1793137
rs1793137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN4B. Location: chromosome 11, position 118,016,068. Clinical significance in the table: Benign.
Reference-table entries
SCN4BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:118016068
- Cytoband
- 11q23.3
- HGVS
- NM_174934.4(SCN4B):c.62-124G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.