Gene entry
SERPINA7
serpin family A member 7
- Chromosome
- X
- Cytoband
- Xq22.3
- Variants (rsID)
- 14
SERPINA7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq22.3). Its official name is “serpin family A member 7”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs121909496Associationsingle nucleotide variantThyroxine-binding globulin quantitative trait locus
- rs28933688Associationsingle nucleotide variantThyroxine-binding globulin quantitative trait locus
- rs28937312Associationsingle nucleotide variantThyroxine-binding globulin quantitative trait locus
- rs72554659Associationsingle nucleotide variantThyroxine-binding globulin deficiency, partial
- rs1804495Benignsingle nucleotide variantThyroxine-binding globulin, variant P|Thyroxine-binding globulin quantitative trait locus
- rs2234036Conflicting interpretationssingle nucleotide variantThyroxine-binding globulin, variant A|Thyroxine-binding globulin deficiency
- rs1050086Pathogenicsingle nucleotide variantThyroxine-binding globulin, slow
- rs28933689Pathogenicsingle nucleotide variantThyroxine-binding globulin deficiency, partial
- rs61754490Pathogenicsingle nucleotide variantThyroxine-binding globulin, Chicago
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.