{{Rsnum
|rsid=398123000
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CHD2
|position=92948970
|Gene_s=CHD2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000077773.1
|CLNALLE=1
|CLNDBN=Epileptic encephalopathy, childhood-onset
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN178848:615369
|CLNHGVS=NC_000015.9:g.93492200C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602119.0009
|Disease=Epileptic encephalopathy
|FwdALT=T
|FwdREF=C
|GENEINFO=CHD2:1106
|GENE_ID=1106
|GENE_NAME=CHD2
|REF=C
|RSPOS=93492200
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398123000
}}