{{Rsnum
|rsid=121908947
|Chromosome=20
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DNMT3B
|position=32789007
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNMT3B
}}{{omim
|id=602900
|rsnum=121908947
|variant=0013
}}{{ClinVar
|rsid=121908947
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=31376813
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DNMT3B:1789
|GENE_NAME=DNMT3B
|GENE_ID=1789
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.31376813T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602900.0013
|CLNSIG=5
|CLNCUI=C0398788
|CLNDBN=Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
|Disease=Centromeric instability of chromosomes 1
|CLNACC=RCV000007137.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0398788:242860:2268:234633000
}}