Variant (rsID / SNP)
rs45580436
rs45580436 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,900,093. Clinical significance in the table: Benign.
Reference-table entries
MYH7Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:23900093
- Cytoband
- 14q11.2
- HGVS
- NM_000257.4(MYH7):c.895+17G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hypertrophic cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.