{{Rsnum
|rsid=2107595
|Chromosome=7
|position=19009765
|Orientation=minus
|GMAF=0.2401
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TWIST1
|Gene_s=TWIST1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 61.5 | 38.5 | 0.0
| HCB | 47.7 | 43.2 | 9.1
| JPT | 26.7 | 57.8 | 15.6
| YRI | 59.7 | 35.5 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 47.7 | 43.2 | 9.1
| 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
}}{{PMID Auto GWAS
  |PMID=23041239
  |Trait=Stroke (ischemic)
  |Title=Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
  |RiskAllele=A
  |Pval=4E-6
  |OR=1.12
  |ORtxt=[1.07-1.17]
  |OA=1
}}

{{PMID Auto
|PMID=23449258
|Title=Evidence HDAC9 Genetic Variant Associated With Ischemic Stroke Increases Risk via Promoting Carotid Atherosclerosis
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease or large artery stroke
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=
  |Pval=3E-12
  |OR=NR
  |ORtxt=NR
  }}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}