Variant (rsID / SNP)
rs16907355
rs16907355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SBF2. Location: chromosome 11, position 10,019,879. Clinical significance in the table: Benign.
Reference-table entries
SBF2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:10019879
- Cytoband
- 11p15.4
- HGVS
- NM_030962.4(SBF2):c.909C>T (p.Pro303=)
- Allele change
- Synonymous_P303P
Associated conditions / phenotypes
Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.