rs35608448
This variant is located in the SLF2 gene.
▶ClinVar annotation
Conflicting Classifications
2 submitters1 publicationnot provided; Inborn genetic diseases
View on ClinVar →About SLF2
Enables ubiquitin protein ligase binding activity. Involved in several processes, including positive regulation of cellular component organization; positive regulation of double-strand break repair; and protein localization to site of double-strand break. Located in PML body; chromatin; and site of double-strand break. Implicated in mosaic variegated aneuploidy syndrome. [provided by Alliance of Genome Resources, Jul 2025]
View all SLF2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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