Gene entry
AVPR2
arginine vasopressin receptor 2
- Chromosome
- X
- Cytoband
- Xq28
- Variants (rsID)
- 32
AVPR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq28). Its official name is “arginine vasopressin receptor 2”. The reference table lists 32 variants (rsID) for this gene.
Clinically classified variants
29 reference-table entries with clinical significance.
- rs2071126Benignsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs5196Benignsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs5200Benignsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs5201Benignsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked|Nephrogenic syndrome of inappropriate antidiuresis
- rs104894760Likely pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked|Nephrogenic diabetes insipidus|Nephrogenic syndrome of inappropriate antidiuresis|Diabetes insipidus, nephrogenic, X-linked
- rs193922112Likely pathogenicsingle nucleotide variantNephrogenic diabetes insipidus
- rs193922113Likely pathogenicsingle nucleotide variantNephrogenic diabetes insipidus
- rs193922114Likely pathogenicDeletionNephrogenic diabetes insipidus
- rs193922115Likely pathogenicDeletionNephrogenic diabetes insipidus
- rs193922117Likely pathogenicsingle nucleotide variantNephrogenic diabetes insipidus
- rs193922118Likely pathogenicDeletionNephrogenic diabetes insipidus
- rs193922119Likely pathogenicDeletionNephrogenic diabetes insipidus
- rs193922120Likely pathogenicDeletionNephrogenic diabetes insipidus
- rs193922122Likely pathogenicsingle nucleotide variantNephrogenic diabetes insipidus
- rs193922123Likely pathogenicsingle nucleotide variantNephrogenic diabetes insipidus
- rs104894747Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894748Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894749Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked|Nephrogenic diabetes insipidus
- rs104894750Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894751Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894752Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894753Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894754Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894755Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894757Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894759Pathogenicsingle nucleotide variantDiabetes insipidus, nephrogenic, X-linked
- rs104894761Pathogenicsingle nucleotide variantNephrogenic syndrome of inappropriate antidiuresis
- rs193922116PathogenicDeletionNephrogenic diabetes insipidus
- rs193922121PathogenicDuplicationNephrogenic diabetes insipidus
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.