Variant (rsID / SNP)
rs3756721
rs3756721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEGF10. Location: chromosome 5, position 126,795,159. Clinical significance in the table: Benign.
Reference-table entries
MEGF10Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:126795159
- Cytoband
- 5q23.2
- HGVS
- NM_001256545.2(MEGF10):c.*2149G>A
- Allele change
- Silent
Associated conditions / phenotypes
MEGF10-Related Myopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.