{{Rsnum
|rsid=121908926
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=AGPAT2
|position=136676603
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGPAT2
}}{{omim
|id=603100
|rsnum=121908926
|variant=0008
}}{{ClinVar
|rsid=121908926
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=139571055
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=AGPAT2:10555
|GENE_NAME=AGPAT2
|GENE_ID=10555
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.139571055G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603100.0008
|CLNSIG=5
|CLNCUI=C1720862
|CLNDBN=Congenital generalized lipodystrophy type 1
|Disease=Congenital generalized lipodystrophy type 1
|CLNACC=RCV000007010.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1212:C1720862:608594:528
}}