{{Rsnum
|rsid=121434437
|Gene=ACVR2B
|Chromosome=3
|position=38477353
|Orientation=plus
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ACVR2B
}}{{omim
|id=602730
|rsnum=121434437
|variant=0001
}}{{ClinVar
|rsid=121434437
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=38518844
|CHROM=3
|GMAF=0.0027
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=ACVR2B:93
|GENE_NAME=ACVR2B
|GENE_ID=93
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38518844G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602730.0001
|CLNSIG=5
|CLNCUI=C3151057
|CLNDBN=Heterotaxy, visceral, 4, autosomal
|Disease=Heterotaxy
|CLNACC=RCV000007261.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151057:613751:450
|COMMON=1
}}