{{Rsnum
|rsid=121909295
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SGCD
|position=156595042
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SGCD
}}{{omim
|id=601411
|rsnum=121909295
|variant=0002
}}{{ClinVar
|rsid=121909295
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156022052
|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.156022052C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601411.0002
|CLNSIG=5
|CLNCUI=C1832525
|CLNDBN=Limb-girdle muscular dystrophy, type 2F
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000008650.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1408:C1832525:601287:219
}}