Gene entry

TNFSF12-TNFSF13

TNFSF12-TNFSF13 readthrough

Chromosome: 17
Cytoband: 17p13.1
Variants (rsID): 1

TNFSF12-TNFSF13 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.1). Its official name is “TNFSF12-TNFSF13 readthrough”. The reference table lists 1 variant (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs3803800Not classifiedmissense_variantIga Glomerulonephritis|Immunoglobulin Alpha Deficiency|Systemic Lupus Erythematosus|Lupus Erythematosus|Glomerulonephritis|Proteinuria, Chronic Benign|Autoimmune Disease|Leukemia, Chronic Lymphocytic|End Stage Renal Disease

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.