{{Rsnum
|rsid=398122812
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FLNA
|position=154348897
|Gene_s=FLNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000022819.15
|CLNALLE=1
|CLNDBN=X-linked periventricular heterotopia
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1213:NBK1393:C1848213:300049:2149:448227009
|CLNHGVS=NC_000023.10:g.153577265C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300017.0034
|Disease=X-linked periventricular heterotopia
|FwdALT=A
|FwdREF=G
|GENEINFO=FLNA:2316
|GENE_ID=2316
|GENE_NAME=FLNA
|REF=C
|RSPOS=153577265
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122812
}}