{{Rsnum
|rsid = 28940572
|Gene = A4GALT
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=22
|position=42693392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=A4GALT
}}{{omim
|desc=P BLOOD GROUP SYSTEM, p PHENOTYPE
|id=607922
|rsnum=28940572
|variant=0004
}}
{{ neighbor
| rsid = 28940571
| distance = 192
}}

{{ClinVar
|rsid=28940572
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=43089398
|CHROM=22
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=A4GALT:53947
|GENE_NAME=A4GALT
|GENE_ID=53947
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.43089398C>T
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000002814.1
|CLNDBN=p phenotype
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0599990:111400:24403008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607922.0004
|Disease=p phenotype
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}