{{Rsnum
|rsid=104894655
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TCAP
|position=39665762
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TCAP
}}{{omim
|id=604488
|rsnum=104894655
|variant=0001
}}{{ClinVar
|rsid=104894655
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37822015
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TCAP:8557
|GENE_NAME=TCAP
|GENE_ID=8557
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.37822015C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604488.0001
|CLNSIG=5
|CLNCUI=C1866008
|CLNDBN=Limb-girdle muscular dystrophy, type 2G; Primary dilated cardiomyopathy
|Disease=Limb-girdle muscular dystrophy; Primary dilated cardiomyopathy
|CLNACC=RCV000005861.1; RCV000037790.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1866008:601954:34514; NBK1309:C0007193:212110:195021004
}}