{{Rsnum
|rsid=104893683
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=B3GALNT1
|position=161085944
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=B3GALNT1
}}{{omim
|id=603094
|rsnum=104893683
|variant=0003
}}{{ClinVar
|rsid=104893683
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=160803732
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=B3GALNT1:8706
|GENE_NAME=B3GALNT1
|GENE_ID=8706
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.160803732C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603094.0003
|CLNSIG=5
|CLNCUI=CN068995
|CLNDBN=p phenotype
|Disease=p phenotype
|CLNACC=RCV000007014.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0599990:111400:24403008
}}