{{Rsnum
|rsid=121908445
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CNTNAP2
|position=148147542
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNTNAP2
}}{{omim
|id=604569
|rsnum=121908445
|variant=0004
}}{{ClinVar
|rsid=121908445
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=147844634
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CNTNAP2:26047
|GENE_NAME=CNTNAP2
|GENE_ID=26047
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.147844634T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604569.0004
|CLNSIG=255
|CLNCUI=C2677504
|CLNDBN=Autism 15
|Disease=Autism 15
|CLNACC=RCV000005828.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2677504:612100
}}