Variant (rsID / SNP)
rs200883903
rs200883903 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,858,735. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
MYH6Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:23858735
- Cytoband
- 14q11.2
- HGVS
- NM_002471.4(MYH6):c.3860-15T>G
- Allele change
- Silent
Associated conditions / phenotypes
Hypertrophic cardiomyopathy 14
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.