{{Rsnum
|rsid=1800578
|Chromosome=20
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=THBD
|position=23048022
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=THBD
}}{{omim
|id=188040
|rsnum=1800578
|variant=0007
}}

{{ClinVar
|rsid=1800578
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=23028659
|CHROM=20
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050168000000040102110100
|GENEINFO=THBD:7056
|GENE_NAME=THBD
|GENE_ID=7056
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.23028659G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188040.0007
|CLNSIG=255
|CLNCUI=C2752036
|CLNDBN=Atypical hemolytic-uremic syndrome 6
|Disease=Atypical hemolytic-uremic syndrome 6
|CLNACC=RCV000013557.1
|Tags=RV;PM;PMC;SLO;VLD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1367:C2752036:612926
}}

{{PMID Auto
|PMID=17677000
|Title=Combined effects of thrombosis pathway gene variants predict cardiovascular events.
|OA=1
}}

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