{{Rsnum
|rsid=267607100
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TAB2
|position=149378603
|Gene_s=TAB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=6
|CLNACC=RCV000005522.1
|CLNALLE=1
|CLNDBN=Congenital heart disease, multiple types, 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3150216:614980
|CLNHGVS=NC_000006.11:g.149699739C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605101.0002
|Disease=Congenital heart disease
|FwdALT=A
|FwdREF=C
|GENEINFO=TAB2:23118
|GENE_ID=23118
|GENE_NAME=TAB2
|REF=C
|RSPOS=149699739
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607100
}}