Variant (rsID / SNP)
rs1045056
rs1045056 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AATF. Location: chromosome 17, position 35,346,641. The table records no clinical significance for this variant.
Reference-table entries
AATFNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:35346641
- HGVS
- NM_012138.4,c.1245T>C,p.Ser415Ser
- Allele change
- Synonymous_S415S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.