Gene entry
SLFN12L
schlafen family member 12 like
- Chromosome
- 17
- Cytoband
- 17q12
- Variants (rsID)
- 19
SLFN12L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “schlafen family member 12 like”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs12451679Not classifiedmissense_variant
- rs2304968Not classifiedmissense_variantLung Cancer
- rs4796089Not classified5_prime_UTR_variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
