{{Rsnum
|rsid = 28936071
|Gene = EFNB1
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=X
|position=68839729
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EFNB1
}}{{omim
|desc=CRANIOFRONTONASAL SYNDROME
|id=300035
|rsnum=28936071
|variant=0006
}}
{{ neighbor
| rsid = 28936070
| distance = 20
}}

{{ neighbor
| rsid = 28935170
| distance = 2
}}

{{ClinVar
|rsid=28936071
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=68059572
|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.68059572A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300035.0006
|CLNSIG=5
|CLNCUI=C0220767
|CLNDBN=Craniofrontonasal dysplasia
|Disease=Craniofrontonasal dysplasia
|CLNACC=RCV000012477.21
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0220767:304110:1520
}}

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