{{Rsnum
|rsid=137852561
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SYP
|position=49191730
|Gene_s=SYP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=313475
|variant=0004
|rsnum=137852561
}}{{ClinVar
|rsid=137852561
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=49048187
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SYP:6855
|GENE_NAME=SYP
|GENE_ID=6855
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.49048187C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=313475.0004
|CLNSIG=5
|CLNCUI=C2749021
|CLNDBN=Mental retardation, X-linked 96
|Disease=Mental retardation
|CLNACC=RCV000010541.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2749021:300802:777
}}