Variant (rsID / SNP)
rs7853758
rs7853758 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC28A3. Location: chromosome 9, position 86,900,926. Clinical significance in the table: drug_response.
Reference-table entries
SLC28A3Drug response
- Clinical significance (as recorded)
- drug_response
- Variant type
- synonymous_variant
- Chromosome / position
- 9:86900926
- HGVS
- NM_001199633.2,c.1381C>T,p.Leu461Leu
- Allele change
- Silent
Associated conditions / phenotypes
Neutropenia|Leukemia|Lung Cancer|Leukemia, Acute Lymphoblastic|Osteogenic Sarcoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.