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Gene entry

SERPING1

serpin family G member 1

Chromosome
11
Cytoband
11q12.1
Variants (rsID)
9

SERPING1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q12.1). Its official name is “serpin family G member 1”. The reference table lists 9 variants (rsID) for this gene.

Clinically classified variants

4 reference-table entries with clinical significance.

  • rs4926Benignsingle nucleotide variantHereditary angioedema type 1
  • rs185342631Conflicting interpretationssingle nucleotide variantHereditary angioedema type 1|C1 inhibitor deficiency|Hereditary angioedema type 1
  • rs121907948Pathogenicsingle nucleotide variantHereditary C1 esterase inhibitor deficiency - dysfunctional factor|Hereditary angioedema type 1
  • rs28940870Pathogenicsingle nucleotide variantHereditary C1 esterase inhibitor deficiency - dysfunctional factor|Hereditary angioedema type 1

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.