{{Rsnum
|rsid = 28989183
|Gene = BUB1B
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=15
|position=40217580
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BUB1B,PAK6
}}{{omim
|desc=MOSAIC VARIEGATED ANEUPLOIDY SYNDROME
|id=602860
|rsnum=28989183
|variant=0005
}}

{{ClinVar
|rsid=28989183
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=40509781
|CHROM=15
|dbSNPBuildID=125
|SSR=0
|SAO=1
|VP=0x050060000000000502110100
|GENEINFO=BUB1B:701; PAK6:56924
|GENE_NAME=BUB1B; PAK6
|GENE_ID=701; 56924
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.40509781G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602860.0005
|CLNSIG=5
|CLNCUI=C1850343; C1864389
|CLNDBN=Mosaic variegated aneuploidy syndrome; Premature chromatid separation trait
|Disease=Mosaic variegated aneuploidy syndrome; Premature chromatid separation trait
|CLNACC=RCV000007156.1; RCV000007157.1
|Tags=PM;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=C1850343:257300:1052; C1864389:176430
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}