{{Rsnum
|rsid=397514502
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=A4GALT
|position=42693321
|Gene_s=A4GALT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=22
|CLNACC=RCV000032632.1
|CLNALLE=1
|CLNDBN=p phenotype
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0599990:111400:24403008
|CLNHGVS=NC_000022.10:g.43089327G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607922.0008
|Disease=p phenotype
|FwdALT=G
|FwdREF=C
|GENEINFO=A4GALT:53947
|GENE_ID=53947
|GENE_NAME=A4GALT
|REF=G
|RSPOS=43089327
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514502
}}