Variant (rsID / SNP)
rs4294629
rs4294629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NANOG. Location: chromosome 12, position 7,945,559. The table records no clinical significance for this variant.
Reference-table entries
NANOGNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:7945559
- HGVS
- NM_024865.4,c.165T>C,p.Pro55Pro
- Allele change
- Synonymous_P55P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.