Gene entry
LPIN2
lipin 2
- Chromosome
- 18
- Cytoband
- 18p11.31
- Variants (rsID)
- 26
LPIN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18p11.31). Its official name is “lipin 2”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs104895501Benignsingle nucleotide variantMajeed syndrome|Psoriasis|Autoinflammatory syndrome
- rs113346639Benignsingle nucleotide variantMajeed syndrome
- rs144555528Benignsingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs17555442Benignsingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs17886056Benignsingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs104895500Conflicting interpretationssingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs80338805Conflicting interpretationssingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs80338807Conflicting interpretationssingle nucleotide variantMajeed syndrome|Autoinflammatory syndrome
- rs183821298Uncertain significancesingle nucleotide variantMajeed syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.