{{Rsnum
|rsid=137853311
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FLNA
|position=154364582
|Gene_s=FLNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300017
|variant=0006
|rsnum=137853311
}}{{ClinVar
|rsid=137853311
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153592950
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FLNA:2316
|GENE_NAME=FLNA
|GENE_ID=2316
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153592950G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300017.0006
|CLNSIG=5
|CLNCUI=C1848213
|CLNDBN=X-linked periventricular heterotopia
|Disease=X-linked periventricular heterotopia
|CLNACC=RCV000012518.21
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1213:NBK1393:C1848213:300049:2149:448227009
}}