{{Rsnum
|rsid=137852971
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=BSCL2
|position=62692413
|Gene_s=BSCL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606158
|variant=0009
|rsnum=137852971
}}{{ClinVar
|rsid=137852971
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=62459885
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HNRNPUL2-BSCL2:100534595; BSCL2:26580
|GENE_NAME=HNRNPUL2-BSCL2; BSCL2
|GENE_ID=100534595; 26580
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.62459885C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606158.0009
|CLNSIG=5
|CLNCUI=C1720863
|CLNDBN=Congenital generalized lipodystrophy type 2
|Disease=Congenital generalized lipodystrophy type 2
|CLNACC=RCV000004797.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1212:C1720863:269700:528
}}