{{Rsnum
|rsid=145100473
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCO2
|position=50524071
|Gene_s=NCAPH2,SCO2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=22
|CLNACC=RCV000043620.1
|CLNALLE=1
|CLNDBN=Myopia 6
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1837148:608908
|CLNHGVS=NC_000022.10:g.50962500C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604272.0009
|Disease=Myopia 6
|FwdALT=T
|FwdREF=C
|GENEINFO=SCO2:9997; NCAPH2:29781
|GENE_ID=9997; 29781
|GENE_NAME=SCO2; NCAPH2
|REF=C
|RSPOS=50962500
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000040002110100
|WGT=0
|dbSNPBuildID=134
|rsid=145100473
}}