{{Rsnum
|rsid=397514557
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=GRIN2A
|position=9829485
|Gene_s=GRIN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000032866.27
|CLNALLE=1
|CLNDBN=Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1832814:245570:1945:725
|CLNHGVS=NC_000016.9:g.9923342G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=138253.0003
|Disease=Rolandic epilepsy
|FwdALT=G
|FwdREF=C
|GENEINFO=GRIN2A:2903
|GENE_ID=2903
|GENE_NAME=GRIN2A
|REF=G
|RSPOS=9923342
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514557
}}