Variant (rsID / SNP)
rs1056664
rs1056664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MELTF. Location: chromosome 3, position 196,746,629. The table records no clinical significance for this variant.
Reference-table entries
MELTFNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:196746629
- HGVS
- NM_033316.4,c.756A>G,p.Glu252Glu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.