{{Rsnum
|rsid=121434333
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MAN2B1
|position=12658470
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAN2B1
}}{{omim
|id=609458
|rsnum=121434333
|variant=0005
}}{{ClinVar
|rsid=121434333
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=12769284
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MAN2B1:4125
|GENE_NAME=MAN2B1
|GENE_ID=4125
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.12769284G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609458.0005
|CLNSIG=5
|CLNCUI=C0024748
|CLNDBN=Deficiency of alpha-mannosidase
|Disease=Deficiency of alpha-mannosidase
|CLNACC=RCV000001756.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1396:C0024748:248500:61:124466001
}}