{{Rsnum
|rsid=193929392
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HCCS
|position=11118574
|Gene_s=HCCS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000020630.1
|CLNALLE=1
|CLNDBN=Microphthalmia syndromic 7
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK7041:C0796070:309801:2556
|CLNHGVS=NC_000023.10:g.11136694G>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK7041
|Disease=Microphthalmia syndromic 7
|FwdALT=A
|FwdREF=G
|GENEINFO=HCCS:3052
|GENE_ID=3052
|GENE_NAME=HCCS
|REF=G
|RSPOS=11136694
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=193929392
}}