{{Rsnum
|rsid=28934600
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=MAN2B1
|position=12665756
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAN2B1,WDR83
}}{{omim
|id=609458
|rsnum=28934600
|variant=0001
}}

{{ClinVar
|rsid=28934600
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=12776570
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=WDR83:84292; MAN2B1:4125
|GENE_NAME=WDR83; MAN2B1
|GENE_ID=84292; 4125
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.12776570T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000001752.1
|CLNDBN=Deficiency of alpha-mannosidase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1396:C0024748:248500:61:124466001
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609458.0001
|Disease=Deficiency of alpha-mannosidase
}}

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