{{Rsnum
|rsid=121918363
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SRPX2
|position=100667292
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SRPX2
}}{{omim
|id=300642
|rsnum=121918363
|variant=0001
}}{{ClinVar
|rsid=121918363
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=99922289
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=SRPX2:27286
|GENE_NAME=SRPX2
|GENE_ID=27286
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.99922289A>G
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=15934; 300642.0001
|CLNSIG=5
|CLNCUI=C1845070
|CLNDBN=X-linked rolandic epilepsy with mental retardation and speech dyspraxia; not provided
|Disease=X-linked rolandic epilepsy with mental retardation and speech dyspraxia; not provided
|CLNACC=RCV000011522.6; RCV000081635.1
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1845070:300643
}}