{{Rsnum
|rsid = 28935174
|Gene = EBP
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=X
|position=48527256
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EBP
}}{{omim
|desc=CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT
|id=300205
|rsnum=28935174
|variant=0012
}}

{{ population diversity
| geno1 = (A;G)
| geno2 = (G;G)
| geno3 = 
| CEU | 0 | 0 | 0
| HCB | 0 | 0 | 0
| JPT | 0 | 0 | 0
| YRI | 0 | 0 | 0
| ASW | 2.1 | 97.9 | 0
| CHD | 0 | 0 | 0
| GIH | 0 | 0 | 0
| LWK | 0 | 0 | 0
| MEX | 0 | 0 | 0
| MKK | 0 | 0 | 0
| TSI | 0 | 0 | 0
}}{{ClinVar
|rsid=28935174
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=48385644
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000000402110100
|GENEINFO=EBP:10682
|GENE_NAME=EBP
|GENE_ID=10682
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.48385644G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300205.0012
|CLNSIG=5
|CLNCUI=C0282102
|CLNDBN=Chondrodysplasia punctata 2 X-linked dominant
|Disease=Chondrodysplasia punctata 2 X-linked dominant
|CLNACC=RCV000012247.10
|Tags=PM;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1291:NBK55062:C0282102:302960:35173
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}