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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.

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.