{{Rsnum
|rsid=121918315
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SYNGAP1
|position=33432709
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SYNGAP1
}}{{omim
|id=603384
|rsnum=121918315
|variant=0001
}}{{ClinVar
|ALT=T
|CHROM=6
|CLNACC=RCV000006764.1
|CLNALLE=1
|CLNDBN=Mental retardation, autosomal dominant 5
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2675473:612621
|CLNHGVS=NC_000006.11:g.33400486A>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603384.0001
|Disease=Mental retardation
|FwdALT=T
|FwdREF=A
|GENEINFO=SYNGAP1:8831
|GENE_ID=8831
|GENE_NAME=SYNGAP1
|REF=A
|RSPOS=33400486
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121918315
}}