{{Rsnum
|rsid=121918364
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SRPX2
|position=100662227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SRPX2
}}{{omim
|id=300642
|rsnum=121918364
|variant=0002
}}{{ClinVar
|rsid=121918364
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=99917224
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SRPX2:27286
|GENE_NAME=SRPX2
|GENE_ID=27286
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.99917224A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300642.0002
|CLNSIG=5
|CLNCUI=C1845070
|CLNDBN=X-linked rolandic epilepsy with mental retardation and speech dyspraxia
|Disease=X-linked rolandic epilepsy with mental retardation and speech dyspraxia
|CLNACC=RCV000011523.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1845070:300643
}}