{{Rsnum
|rsid=80338807
|Chromosome=18
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LPIN2
|position=2922173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LPIN2
}}{{omim
|id=605519
|rsnum=80338807
|variant=0001
}}{{ClinVar
|rsid=80338807
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=2922171
|CHROM=18
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=LPIN2:9663
|GENE_NAME=LPIN2
|GENE_ID=9663
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.2922171G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=0
|CLNSRCID=NBK1974; 605519.0001; 404
|CLNSIG=5
|CLNCUI=C1864997; C1864997
|CLNDBN=Majeed syndrome
|Disease=Majeed syndrome
|CLNACC=RCV000005190.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1974:C1864997:609628:77297
}}{{PMID Auto
|PMID=2809904
|Title=Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children and the association with Sweet syndrome in two siblings.
}}

{{PMID Auto
|PMID=10969284
|Title=On mice and men: An autosomal recessive syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia.
}}

{{PMID Auto
|PMID=15994876
|Title=Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).
|OA=1
}}