Variant (rsID / SNP)
rs183611755
rs183611755 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH6. Location: chromosome 14, position 23,876,437. Clinical significance in the table: Benign.
Reference-table entries
MYH6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:23876437
- Cytoband
- 14q11.2
- HGVS
- NM_002471.4(MYH6):c.-5C>A
- Allele change
- Silent
Associated conditions / phenotypes
Cardiovascular phenotype|Cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.