{{Rsnum
|rsid=397514584
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COX7B
|position=77902641
|Gene_s=COX7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=X
|CLNACC=RCV000032987.5
|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.77158138A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300885.0002
|Disease=Aplasia cutis congenita
|FwdALT=G
|FwdREF=A
|GENEINFO=COX7B:1349
|GENE_ID=1349
|GENE_NAME=COX7B
|REF=A
|RSPOS=77158138
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514584
}}