{{Rsnum
|rsid=104894802
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=EFNB1
|position=68829885
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EFNB1
}}{{omim
|id=300035
|rsnum=104894802
|variant=0008
}}{{ClinVar
|rsid=104894802
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=68049728
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=EFNB1:1947
|GENE_NAME=EFNB1
|GENE_ID=1947
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.68049728T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300035.0008
|CLNSIG=5
|CLNCUI=C0220767
|CLNDBN=Craniofrontonasal dysplasia
|Disease=Craniofrontonasal dysplasia
|CLNACC=RCV000012479.15
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0220767:304110:1520
}}