{{Rsnum
|rsid = 28934568
|Gene = TGFBR2
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=3
|position=30672106
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TGFBR2
}}{{omim
|desc=MARFAN SYNDROME, TYPE II
|id=190182
|rsnum=28934568
|variant=0005
}}

{{ClinVar
|rsid=28934568
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=30713598
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TGFBR2:7048
|GENE_NAME=TGFBR2
|GENE_ID=7048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.30713598T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=190182.0005
|CLNSIG=5
|CLNCUI=C2674574; C2674876
|CLNDBN=Loeys-Dietz syndrome type 2B; Loeys-Dietz syndrome type 1B
|Disease=Loeys-Dietz syndrome type 2B; Loeys-Dietz syndrome type 1B
|CLNACC=RCV000013328.23; RCV000013329.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1133:C2674574:610380:284973:558; NBK1133:C2674876:610168:60030
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}