{{Rsnum
|rsid=281875230
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SMARCA4
|position=11030816
|Gene_s=SMARCA4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=19
|CLNACC=RCV000023289.1; RCV000059688.1
|CLNALLE=1
|CLNDBN=Mental retardation, autosomal dominant 16; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN123924:614609:1465
|CLNHGVS=NC_000019.9:g.11141492C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=603254.0007; VAR_068214
|Disease=Mental retardation; not provided
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=11141492
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875230
|GENEINFO=SMARCA4:6597
|GENE_ID=6597
|GENE_NAME=SMARCA4
}}{{PMID Auto
|PMID=22426308
|Title=Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
}}