Gene entry
PXDN
peroxidasin
- Chromosome
- 2
- Cytoband
- 2p25.3
- Variants (rsID)
- 42
PXDN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p25.3). Its official name is “peroxidasin”. The reference table lists 42 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs17841813Benignsingle nucleotide variantAnterior segment dysgenesis 7
- rs202132697Benignsingle nucleotide variantDevelopmental cataract|Anterior segment dysgenesis 7
- rs6723697Benignsingle nucleotide variantAnterior segment dysgenesis 7
- rs7578605Benignsingle nucleotide variantAnterior segment dysgenesis 7
Other listed variants
- rs2278114
- rs4853759
- rs4853841
- rs4853849
- rs6548062
- rs6710867
- rs6714537
- rs7588729
- rs7589213
- rs7601211
- rs9917191
- rs10180168
- rs13393011
- rs17038986
- rs28577916
- rs55745268
- rs56183650
- rs58238766
- rs62116593
- rs62116633
- rs72765517
- rs73178775
- rs73910831
- rs73910866
- rs75689376
- rs77493634
- rs77824171
- rs79802891
- rs114356459
- rs114360452
- rs117207020
- rs142336871
- rs181285160
- rs183629867
- rs188971798
- rs199555155
- rs201763004
- rs374907262
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
