{{Rsnum
|rsid=119480072
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LPIN1
|position=11783834
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LPIN1
}}{{omim
|id=605518
|rsnum=119480072
|variant=0002
}}{{ClinVar
|rsid=119480072
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=11923960
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LPIN1:23175
|GENE_NAME=LPIN1
|GENE_ID=23175
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.11923960C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605518.0002
|CLNSIG=5
|CLNCUI=CN068857
|CLNDBN=Myoglobinuria, recurrent, autosomal recessive
|Disease=Myoglobinuria
|CLNACC=RCV000005193.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN068857
}}