{{Rsnum
|rsid=104894919
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PHF6
|position=134415055
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PHF6
}}{{omim
|id=300414
|rsnum=104894919
|variant=0007
}}{{ClinVar
|rsid=104894919
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=133549085
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PHF6:84295
|GENE_NAME=PHF6
|GENE_ID=84295
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.133549085A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300414.0007
|CLNSIG=5
|CLNCUI=C0265339
|CLNDBN=Borjeson-Forssman-Lehmann syndrome
|Disease=Borjeson-Forssman-Lehmann syndrome
|CLNACC=RCV000011818.4
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265339:301900:127:21634003
}}