Variant (rsID / SNP)
rs2677879
rs2677879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to METTL4. Location: chromosome 18, position 2,547,500. The table records no clinical significance for this variant.
Reference-table entries
METTL4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:2547500
- HGVS
- NM_022840.5,c.928C>A,p.Gln310Lys
- Allele change
- Missense_Q310K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.