{{Rsnum
|rsid=200533370
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SYN1
|position=47574285
|Gene_s=SYN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000034817.3
|CLNALLE=1
|CLNDBN=Epilepsy, X-linked, with variable learning disabilities and behavior disorders
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845343:300491:85294
|CLNHGVS=NC_000023.10:g.47433684T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=313440.0004
|Disease=Epilepsy
|FwdALT=C
|FwdREF=T
|GENEINFO=SYN1:6853
|GENE_ID=6853
|GENE_NAME=SYN1
|REF=T
|RSPOS=47433684
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=200533370
}}