Variant (rsID / SNP)
rs116500162
rs116500162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEGF10. Location: chromosome 5, position 126,781,311. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
MEGF10Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:126781311
- Cytoband
- 5q23.2
- HGVS
- NM_001256545.2(MEGF10):c.2654G>A (p.Gly885Glu)
- Allele change
- Missense_G885E
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.