Variant (rsID / SNP)
rs72552198
rs72552198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN3B. Location: chromosome 11, position 123,503,998. Clinical significance in the table: Benign.
Reference-table entries
SCN3BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:123503998
- Cytoband
- 11q24.1
- HGVS
- NM_001040151.2(SCN3B):c.*509G>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.