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SLFN12L

schlafen family member 12 like

HCNC Approved Symbol
SLFN12L (HGNC:33920)
Genomic Coordinates
17:35,464,254 - 35,537,678 (17q12)
Synonyms
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

SLFN12L - Gene browser | 3billion