{{Rsnum
|rsid=137853316
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FLNA
|position=154354860
|Gene_s=FLNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300017
|variant=0022
|rsnum=137853316
}}{{ClinVar
|rsid=137853316
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=153583228
|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.153583228C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000012534.21
|CLNDBN=Otopalatodigital spectrum disorder
|CLNDSDB=MedGen
|CLNDSDBID=C2748918
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300017.0022
|Disease=Otopalatodigital spectrum disorder
}}