{{Rsnum
|rsid=132630324
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PCDH19
|position=100408345
|Gene_s=PCDH19
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300460
|variant=0003
|rsnum=132630324
}}{{ClinVar
|rsid=132630324
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=99663343
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PCDH19:57526
|GENE_NAME=PCDH19
|GENE_ID=57526
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.99663343G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300460.0003
|CLNSIG=5
|CLNCUI=C1848137
|CLNDBN=Early infantile epileptic encephalopathy 9
|Disease=Early infantile epileptic encephalopathy 9
|CLNACC=RCV000011764.8
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1848137:300088:2076
}}