Gene entry
PEPD
peptidase D
- Chromosome
- 19
- Cytoband
- 19q13.11
- Variants (rsID)
- 40
PEPD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.11). Its official name is “peptidase D”. The reference table lists 40 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs2230062Benignsingle nucleotide variantProlidase deficiency
- rs3745969Benignsingle nucleotide variantProlidase deficiency
- rs74988985Benignsingle nucleotide variantProlidase deficiency
- rs121917723Likely pathogenicsingle nucleotide variantProlidase deficiency
- rs267606943Pathogenicsingle nucleotide variantProlidase deficiency
- rs745834191PathogenicDeletionProlidase deficiency
Other listed variants
- rs33823
- rs33837
- rs33842
- rs153508
- rs731839
- rs889140
- rs3786897
- rs3786916
- rs4362488
- rs4805885
- rs6510385
- rs7250175
- rs8105921
- rs8107100
- rs8107339
- rs8111294
- rs13343443
- rs17760904
- rs73035072
- rs73037106
- rs76690849
- rs76885489
- rs77091279
- rs78820813
- rs78958855
- rs112860861
- rs113160575
- rs116780918
- rs117113997
- rs117283488
- rs117684449
- rs117699443
- rs117903521
- rs139214756
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.