{{Rsnum
|rsid=137852560
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SYN1
|position=47576222
|Gene_s=SYN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=313440
|variant=0001
|rsnum=137852560
}}{{ClinVar
|rsid=137852560
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=47435621
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SYN1:6853
|GENE_NAME=SYN1
|GENE_ID=6853
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.47435621C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=313440.0001
|CLNSIG=5
|CLNCUI=C1845343
|CLNDBN=Epilepsy, X-linked, with variable learning disabilities and behavior disorders
|Disease=Epilepsy
|CLNACC=RCV000010542.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845343:300491:85294
}}