Gene entry
PLCG2
phospholipase C gamma 2
- Chromosome
- 16
- Cytoband
- 16q23.3
- Variants (rsID)
- 89
PLCG2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q23.3). Its official name is “phospholipase C gamma 2”. The reference table lists 89 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs1071644Benignsingle nucleotide variantFamilial cold autoinflammatory syndrome 3|Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
- rs1143687Benignsingle nucleotide variantFamilial cold autoinflammatory syndrome 3
- rs114618894Benignsingle nucleotide variantFamilial cold autoinflammatory syndrome 3|Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
- rs75472618Benignsingle nucleotide variantFamilial cold autoinflammatory syndrome 3
- rs187956469Conflicting interpretationssingle nucleotide variantFamilial cold autoinflammatory syndrome 3
Other listed variants
- rs3935743
- rs4073828
- rs4133125
- rs4243218
- rs4243222
- rs4243225
- rs4243226
- rs4284633
- rs4325546
- rs4369659
- rs4405545
- rs4410068
- rs4420523
- rs4424903
- rs4494535
- rs4499225
- rs4520827
- rs4580153
- rs4888187
- rs4888197
- rs4889384
- rs4889393
- rs4889438
- rs6564923
- rs6564940
- rs7187863
- rs7192266
- rs7201504
- rs8055576
- rs8182116
- rs9928191
- rs9932716
- rs9934030
- rs9937223
- rs9938623
- rs11150418
- rs11640294
- rs11645253
- rs11648625
- rs12446070
- rs12447917
- rs12448334
- rs12919270
- rs12921780
- rs12932861
- rs16956064
- rs34457613
- rs34748139
- rs35142664
- rs41311272
- rs45491692
- rs61068265
- rs62043997
- rs62044062
- rs62046431
- rs72824912
- rs72824930
- rs72824944
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.