Gene entry
PCSK5
proprotein convertase subtilisin/kexin type 5
- Chromosome
- 9
- Cytoband
- 9q21.13
- Variants (rsID)
- 191
PCSK5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q21.13). Its official name is “proprotein convertase subtilisin/kexin type 5”. The reference table lists 191 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs34417623Uncertain significancesingle nucleotide variant
Other listed variants
- rs765468
- rs871449
- rs914256
- rs914366
- rs990560
- rs1023181
- rs1027383
- rs1029034
- rs1029037
- rs1029041
- rs1039034
- rs1110222
- rs1338746
- rs1339236
- rs1339249
- rs1339254
- rs1340500
- rs1340501
- rs1340508
- rs1416548
- rs1475615
- rs1571791
- rs1571792
- rs1587103
- rs1979737
- rs2066188
- rs2153226
- rs2225969
- rs2260649
- rs2261722
- rs2262160
- rs2270570
- rs2275406
- rs2279659
- rs2297342
- rs2377528
- rs2377637
- rs2490592
- rs2777020
- rs2789610
- rs2803408
- rs2803411
- rs2803433
- rs2842467
- rs2842480
- rs2842483
- rs4113091
- rs4391491
- rs4744776
- rs4744780
- rs4744784
- rs4745477
- rs4745507
- rs4745511
- rs4745519
- rs5022354
- rs5898470
- rs6560476
- rs6560490
- rs6560492
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.