Variant (rsID / SNP)
rs45490796
rs45490796 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,897,921. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
MYH7Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- Deletion
- Chromosome / position
- 14:23897921
- Cytoband
- 14q11.2
- HGVS
- NM_000257.4(MYH7):c.1408-42del
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.