{{Rsnum
|rsid=387906279
|Chromosome=22
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CTT)
|geno3=(CTT;CTT)
|Gene=A4GALT
|position=42693710
|Gene_s=A4GALT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=22
|CLNACC=RCV000002815.1
|CLNALLE=1
|CLNDBN=p phenotype
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0599990:111400:24403008
|CLNHGVS=NC_000022.10:g.43089716_43089718delAAG
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607922.0005
|Disease=p phenotype
|FwdREF=TTC
|REF=GAAG
|RSPOS=43089715
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906279
|GENEINFO=A4GALT:53947
|GENE_ID=53947
|GENE_NAME=A4GALT
}}