{{Rsnum
|rsid=56141211
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GCNT2
|position=10626447
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GCNT2
}}{{omim
|id=600429
|rsnum=56141211
|variant=0001
}}

{{ClinVar
|rsid=56141211
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=10626680
|CHROM=6
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GCNT2:2651
|GENE_NAME=GCNT2
|GENE_ID=2651
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.10626680G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000009699.3
|CLNDBN=Adult i Blood Group with or without Congenital Cataract
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1862229:110800
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600429.0001
|Disease=Adult i Blood Group with or without Congenital Cataract
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}