Variant (rsID / SNP)
rs948298
rs948298 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM1. Location: chromosome 18, position 3,089,522. Clinical significance in the table: Benign.
Reference-table entries
MYOM1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 18:3089522
- Cytoband
- 18p11.31
- HGVS
- NM_003803.4(MYOM1):c.4069+13C>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.