{{Rsnum
|rsid=80338808
|Chromosome=18
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LPIN2
|position=2922046
|Gene_s=LPIN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338808
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=2922044
|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.2922044C>G
|CLNSRC=GeneReviews; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=0
|CLNSRCID=NBK1974; 594
|CLNSIG=5
|CLNCUI=C1864997
|CLNDBN=Majeed syndrome
|Disease=Majeed syndrome
|CLNACC=RCV000020709.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1974:C1864997:609628:77297
}}{{PMID Auto
|PMID=17330256
|Title=A splice site mutation confirms the role of LPIN2 in Majeed syndrome.
}}