Variant (rsID / SNP)
rs4789769
rs4789769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OGFOD3. Location: chromosome 17, position 80,373,452. The table records no clinical significance for this variant.
Reference-table entries
OGFOD3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:80373452
- HGVS
- NM_175902.5,c.126G>A,p.Pro42Pro
- Allele change
- Synonymous_P42P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.