{{Rsnum
|rsid=362277
|Gene=HTT
|Chromosome=4
|position=3217326
|Orientation=minus
|GMAF=0.1869
|Gene_s=HTT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 20.0 | 80.0
| HCB | 0.0 | 6.7 | 93.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 38.1 | 44.4 | 17.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 6.7 | 93.3
| 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
|PMID=22134093
|Title=Polymorphisms and noncardioembolic stroke in three case-control studies
}}{{PMID Auto
|PMID=16391835
|Title=Late-onset and typical Huntington disease families from Crete have distinct genetic origins.
}}