Variant (rsID / SNP)
rs4796089
rs4796089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN12L. Location: chromosome 17, position 33,814,758. The table records no clinical significance for this variant.
Reference-table entries
SLFN12LNot classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 17:33814758
- HGVS
- NM_001195790.3,c.-54A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.