{{Rsnum
|rsid=104893869
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SGCB
|position=52029835
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SGCB
}}{{omim
|id=600900
|rsnum=104893869
|variant=0008
}}
{{omim
|id=600900
|rsnum=104893869
|variant=0005
}}{{ClinVar
|rsid=104893869
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=52896001
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SGCB:6443
|GENE_NAME=SGCB
|GENE_ID=6443
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000004.11:g.52896001C>A; NC_000004.11:g.52896001C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600900.0008; 600900.0005
|CLNSIG=5
|CLNCUI=C1858593
|CLNDBN=Limb-girdle muscular dystrophy, type 2E
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000009257.1; RCV000009254.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858593:604286:119
}}