Gene entry

SLFN12

schlafen family member 12

Chromosome: 17
Cytoband: 17q12
Variants (rsID): 10

SLFN12 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”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs2586514Not classifiedmissense_variant

Other listed variants

rs722375
rs772291
rs997655
rs9889442
rs12940126
rs59538473
rs62078104
rs62081002
rs117276112

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.