{{Rsnum
|rsid=137853266
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FGD1
|position=54467796
|Gene_s=FGD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300546
|variant=0009
|rsnum=137853266
}}{{ClinVar
|rsid=137853266
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=54494229
|CHROM=X
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGD1:2245
|GENE_NAME=FGD1
|GENE_ID=2245
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.54494229C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300546.0009
|CLNSIG=5
|CLNCUI=C0175701
|CLNDBN=Aarskog syndrome
|Disease=Aarskog syndrome
|CLNACC=RCV000011579.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0175701:305400:915:14921002
}}