{{Rsnum
|rsid=137852915
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EPM2A
|position=145686276
|Gene_s=EPM2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607566
|variant=0003
|rsnum=137852915
}}{{ClinVar
|rsid=137852915
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=146007412
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=EPM2A:7957
|GENE_NAME=EPM2A
|GENE_ID=7957
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.146007412G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607566.0003
|CLNSIG=5
|CLNCUI=C0751783
|CLNDBN=Lafora disease
|Disease=Lafora disease
|CLNACC=RCV000003246.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1389:C0751783:254780:501:230425004
}}