{{Rsnum
|rsid=121917889
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HCCS
|position=11121652
|Gene_s=HCCS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121917889
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=11139772
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=HCCS:3052
|GENE_NAME=HCCS
|GENE_ID=3052
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.11139772C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK7041; 300056.0003
|CLNSIG=5
|CLNCUI=C0796070
|CLNDBN=Microphthalmia, syndromic, 7; Microphthalmia syndromic 7
|Disease=Microphthalmia; Microphthalmia syndromic 7
|CLNACC=RCV000012437.23; RCV000020632.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK7041:C0796070:309801:2556
}}