Variant (rsID / SNP)
rs787666
rs787666 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOF. Location: chromosome 10, position 95,072,906. The table records no clinical significance for this variant.
Reference-table entries
MYOFNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:95072906
- HGVS
- NM_013451.4,c.5760A>G,p.Arg1920Arg
- Allele change
- Synonymous_R1920R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.