Gene entry
WDR72
WD repeat domain 72
- Chromosome
- 15
- Cytoband
- 15q21.3
- Variants (rsID)
- 52
WDR72 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q21.3). Its official name is “WD repeat domain 72”. The reference table lists 52 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs17730281Benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive|Amelogenesis imperfecta hypomaturation type 2A3
- rs4633660Benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive
- rs6416452Benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive|Amelogenesis imperfecta hypomaturation type 2A3
- rs690337Benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive|Amelogenesis imperfecta hypomaturation type 2A3
- rs16966320Likely benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive
- rs34123953Likely benignsingle nucleotide variantAmelogenesis imperfecta hypomaturation type 2A3
- rs60404950Likely benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive
- rs7182198Likely benignsingle nucleotide variantAmelogenesis Imperfecta, Recessive
- rs143816093Pathogenicsingle nucleotide variantAmelogenesis imperfecta hypomaturation type 2A3
Other listed variants
- rs473664
- rs523677
- rs689631
- rs989790
- rs1381194
- rs1906402
- rs2126188
- rs4448885
- rs4625672
- rs6493645
- rs8182039
- rs10220852
- rs10518733
- rs11856406
- rs12708431
- rs12902124
- rs16966276
- rs16966350
- rs17630697
- rs17730436
- rs28609360
- rs72745136
- rs72747331
- rs74666691
- rs75484630
- rs79631823
- rs79708007
- rs79994994
- rs117050511
- rs117165318
- rs118006290
- rs118120057
- rs118175116
- rs140373011
- rs144285622
- rs148487960
- rs181430191
- rs188590145
- rs188890309
- rs193141655
- rs200230209
- rs200822732
- rs370856121
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
