{{Rsnum
|rsid=397518469
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GRIN2A
|position=9849963
|Gene_s=GRIN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000074390.26
|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.9943820T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=138253.0008
|Disease=Rolandic epilepsy
|FwdALT=G
|FwdREF=A
|GENEINFO=GRIN2A:2903
|GENE_ID=2903
|GENE_NAME=GRIN2A
|REF=T
|RSPOS=9943820
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397518469
}}