{{Rsnum
|rsid=397514583
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=COX7B
|position=77905214
|Gene_s=COX7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000032986.4
|CLNALLE=1
|CLNDBN=Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN163066:300887:2556
|CLNHGVS=NC_000023.10:g.77160711delC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300885.0001
|Disease=Aplasia cutis congenita
|FwdREF=C
|GENEINFO=COX7B:1349
|GENE_ID=1349
|GENE_NAME=COX7B
|REF=AC
|RSPOS=77160709
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397514583
}}