{{Rsnum
|rsid=387906718
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGD1
|position=54455497
|Gene_s=FGD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000022866.5
|CLNALLE=1
|CLNDBN=Aarskog syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0175701:305400:915:14921002
|CLNHGVS=NC_000023.10:g.54481930G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300546.0012
|Disease=Aarskog syndrome
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=54481930
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906718
|GENEINFO=FGD1:2245
|GENE_ID=2245
|GENE_NAME=FGD1
}}