Variant (rsID / SNP)
rs12615819
rs12615819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPO. Location: chromosome 2, position 1,544,617. The table records no clinical significance for this variant.
Reference-table entries
TPONot classified
- Variant type
- intron_variant
- Chromosome / position
- 2:1544617
- HGVS
- NM_000547.6,c.2748+122G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.