{{Rsnum
|rsid=137853313
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FLNA
|position=154371130
|Gene_s=FLNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300017
|variant=0019
|rsnum=137853313
}}{{ClinVar
|rsid=137853313
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=153599498
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FLNA:2316
|GENE_NAME=FLNA
|GENE_ID=2316
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153599498G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300017.0019
|CLNSIG=5
|CLNCUI=C1845235
|CLNDBN=Heterotopia, periventricular, Ehlers-Danlos variant
|Disease=Heterotopia
|CLNACC=RCV000012531.13
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845235:300537:82004
}}