{{Rsnum
|rsid=80338806
|Chromosome=18
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=LPIN2
|position=2951104
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LPIN2
}}{{ClinVar
|rsid=80338806
|Reversed=1
|FwdREF=AT
|FwdALT=
|REF=CAT
|ALT=C
|RSPOS=2951101
|CHROM=18
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.2951102_2951103delAT
|CLNSRC=GeneReviews; OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=0
|CLNSRCID=NBK1974; 605519.0002; 405
|CLNSIG=5
|CLNCUI=C1864997; C1864997
|CLNDBN=Majeed syndrome
|Disease=Majeed syndrome
|CLNACC=RCV000005191.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1974:C1864997:609628:77297
|GENEINFO=LPIN2:9663
|GENE_ID=9663
|GENE_NAME=LPIN2
}}{{PMID Auto
|PMID=11795677
|Title=The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a review.
}}

{{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
}}