{{Rsnum
|rsid=80356747
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BAAT
|Gene_s=BAAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=101362718
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000020464.1
|CLNALLE=1
|CLNDBN=Atypical hemolytic-uremic syndrome 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2749604:235400:2134
|CLNHGVS=NC_000009.11:g.104125000T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1367
|Disease=Atypical hemolytic-uremic syndrome 1
|FwdALT=G
|FwdREF=A
|GENEINFO=BAAT:570
|GENE_ID=570
|GENE_NAME=BAAT
|REF=T
|RSPOS=104125000
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80356747
}}{{PMID Auto
|PMID=17182750
|Title=Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome.
|OA=1
}}