{{Rsnum
|rsid=121909298
|Chromosome=5
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SGCD
|position=156595000
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SGCD
}}{{omim
|id=601411
|rsnum=121909298
|variant=0006
}}{{ClinVar
|rsid=121909298
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=156022010
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SGCD:6444
|GENE_NAME=SGCD
|GENE_ID=6444
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.156022010T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601411.0006
|CLNSIG=5
|CLNCUI=C1847667
|CLNDBN=Dilated cardiomyopathy 1L; Muscular dystrophy, limb-girdle, type 2f, digenic; AllHighlyPenetrant
|Disease=Dilated cardiomyopathy 1L; Muscular dystrophy; AllHighlyPenetrant
|CLNACC=RCV000008654.1; RCV000008655.1; RCV000041407.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C1847667:606685:154; CN169374
}}