{{Rsnum
|rsid=397514585
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=COX7B
|position=77902657
|Gene_s=COX7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000032988.1
|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.77158154C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300885.0003
|Disease=Aplasia cutis congenita
|FwdALT=T
|FwdREF=C
|GENEINFO=COX7B:1349
|GENE_ID=1349
|GENE_NAME=COX7B
|REF=C
|RSPOS=77158154
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514585
}}