Variant (rsID / SNP)
rs62328061
rs62328061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to METTL14. Location: chromosome 4, position 119,610,606. The table records no clinical significance for this variant.
Reference-table entries
METTL14Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:119610606
- HGVS
- NM_020961.4,c.237A>G,p.Glu79Glu
- Allele change
- Synonymous_E79E
Associated conditions / phenotypes
Hepatoblastoma|Neuroblastoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.