{{Rsnum
|rsid=387907109
|Chromosome=1
|position=90939340
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ZNF644
|Gene_s=ZNF644
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000024103.1
|CLNALLE=1
|CLNDBN=Myopia 21, autosomal dominant
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3279997:614167
|CLNHGVS=NC_000001.11:g.90939340T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_016620.3:c.23-21186A>G; NM_201269.2:c.2014A>G; 614159.0001
|Disease=Myopia 21
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=90939340
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060080a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387907109
|GENEINFO=ZNF644:84146
|GENE_ID=84146
|GENE_NAME=ZNF644
|CLNORIGIN=1
}}