{{Rsnum
|rsid=28935498
|Gene=FGD1
|Chromosome=X
|position=54470182
|Orientation=minus
|GMAF=0.0006046
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGD1
}}{{omim
|id=300546
|rsnum=28935498
|variant=0005
}}

{{ClinVar
|rsid=28935498
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=54496615
|CHROM=X
|GMAF=0.000602773
|dbSNPBuildID=134
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=FGD1:2245
|GENE_NAME=FGD1
|GENE_ID=2245
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.54496615G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300546.0005
|CLNSIG=5
|CLNCUI=CN069557
|CLNDBN=Syndromic X-linked mental retardation 16
|Disease=Syndromic X-linked mental retardation 16
|CLNACC=RCV000011575.7
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9994; 0.0006046
|CLNDSDB=MedGen
|CLNDSDBID=CN069557
|COMMON=0
}}

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