Gene entry
HNF1B
HNF1 homeobox B
- Chromosome
- 17
- Cytoband
- 17q12
- Variants (rsID)
- 41
HNF1B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “HNF1 homeobox B”. The reference table lists 41 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs2688Benignsingle nucleotide variantRenal cysts and diabetes syndrome
- rs771697321Benignsingle nucleotide variantRenal cysts and diabetes syndrome
- rs141166864Conflicting interpretationssingle nucleotide variantRenal cysts and diabetes syndrome
- rs199572129Conflicting interpretationssingle nucleotide variant
Other listed variants
- rs757210
- rs916895
- rs2074428
- rs2107131
- rs2189303
- rs3744763
- rs4430796
- rs7213333
- rs7223387
- rs7405776
- rs7501939
- rs8064454
- rs11263763
- rs11651496
- rs11651755
- rs11658063
- rs12450628
- rs12935974
- rs35451363
- rs35551980
- rs57315554
- rs74796056
- rs77335578
- rs79882976
- rs121918671
- rs121918673
- rs140562402
- rs193922482
- rs193922483
- rs193922486
- rs193922488
- rs193922489
- rs193922490
- rs193922491
- rs193922492
- rs193922493
- rs576061184
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.