{{Rsnum
|rsid = 28935473
|Gene = FLNA
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=X
|position=154360199
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLNA
}}{{omim
|desc=MELNICK-NEEDLES SYNDROME
|id=300017
|rsnum=28935473
|variant=0013
}}
{{ neighbor
| rsid = 28935472
| distance = 34
}}

{{ClinVar
|rsid=28935473
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153588567
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=FLNA:2316
|GENE_NAME=FLNA
|GENE_ID=2316
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153588567G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1393; 300017.0013
|CLNSIG=5
|CLNCUI=C0025237; C0025237
|CLNDBN=Melnick-Needles syndrome
|Disease=Melnick-Needles syndrome
|CLNACC=RCV000012525.14
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1393:C0025237:309350:2484:13449007
}}

{{PMID Auto
|PMID=12612583
|Title=Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.
}}

{{PMID Auto
|PMID=16538226
|Title=Postzygotic mutation and germline mosaicism in the otopalatodigital syndrome spectrum disorders.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}