{{Rsnum
|rsid=398122998
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CHD2
|position=93020076
|Gene_s=CHD2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000077771.1
|CLNALLE=1
|CLNDBN=Epileptic encephalopathy, childhood-onset
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN178848:615369
|CLNHGVS=NC_000015.9:g.93563306G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602119.0007
|Disease=Epileptic encephalopathy
|FwdALT=A
|FwdREF=G
|GENEINFO=CHD2:1106
|GENE_ID=1106
|GENE_NAME=CHD2
|REF=G
|RSPOS=93563306
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122998
}}