{{Rsnum
|rsid=11567847
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TEAD1
|position=12937202
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TEAD1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=189967
|rsnum=11567847
|variant=0001
}}

{{ClinVar
|rsid=11567847
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=12958749
|CHROM=11
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050060000000000503110100
|GENEINFO=TEAD1:7003
|GENE_NAME=TEAD1
|GENE_ID=7003
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.12958749T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNACC=RCV000013465.21
|CLNDBN=Sveinsson choreoretinal atrophy
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=189967.0001
|Disease=Sveinsson choreoretinal atrophy
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}