{{Rsnum
|rsid=104894423
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SGCG
|position=23324452
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SGCG
}}{{omim
|id=608896
|rsnum=104894423
|variant=0008
}}{{ClinVar
|rsid=104894423
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=23898591
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SGCG:6445
|GENE_NAME=SGCG
|GENE_ID=6445
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.23898591G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=5327; 608896.0008
|CLNSIG=5
|CLNCUI=C0410173
|CLNDBN=Severe autosomal recessive muscular dystrophy of childhood - North African type; Malignant melanoma; not provided
|Disease=Severe autosomal recessive muscular dystrophy of childhood - North African type; Malignant melanoma; not provided
|CLNACC=RCV000002086.1; RCV000070315.2; RCV000078408.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=NBK1408:C0410173:253700:353:240056002; C0025202:2092003
}}