{{Rsnum
|rsid=72544141
|Gene=ANK2
|Chromosome=4
|position=113348277
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ANK2
}}{{omim
|id=106410
|rsnum=72544141
|variant=0001
}}

{{ClinVar
|rsid=72544141
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=114269433
|CHROM=4
|GMAF=0.0014
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050378000000000016110100
|GENEINFO=ANK2:287
|GENE_NAME=ANK2
|GENE_ID=287
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.114269433A>G
|CLNSRC=Cardiovascular Biomedical Research Unit; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001127493.1:c.4373A>G; 106410.0001
|CLNSIG=5
|CLNCUI=C1833154; C1970119
|CLNDBN=Long QT syndrome 4; Cardiac arrhythmia, ankyrin B-related; not provided
|Disease=Long QT syndrome 4; Cardiac arrhythmia; not provided
|CLNACC=RCV000019672.26; RCV000019673.26; RCV000058356.1
|Tags=PM;TPA;PMC;S3D;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=C1833154:101016; C1970119:600919:101016
|COMMON=1
}}

{{PMID|12571597}} Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death.

{{PMID|15178757|OA=1
}} A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.

{{PMID|18832177|OA=1
}} Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease.

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