rs82334
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs82334(A;A) |
| Make rs82334(A;C) |
| Make rs82334(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 3223644 |
| Gene | HTT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs82334 |
| dbSNP (classic) | rs82334 |
| ClinGen | rs82334 |
| ebi | rs82334 |
| HLI | rs82334 |
| Exac | rs82334 |
| Gnomad | rs82334 |
| Varsome | rs82334 |
| LitVar | rs82334 |
| Map | rs82334 |
| PheGenI | rs82334 |
| Biobank | rs82334 |
| 1000 genomes | rs82334 |
| hgdp | rs82334 |
| ensembl | rs82334 |
| geneview | rs82334 |
| scholar | rs82334 |
| rs82334 | |
| pharmgkb | rs82334 |
| gwascentral | rs82334 |
| openSNP | rs82334 |
| 23andMe | rs82334 |
| SNPshot | rs82334 |
| SNPdbe | rs82334 |
| MSV3d | rs82334 |
| GWAS Ctlg | rs82334 |
| GMAF | 0.3108 |
| Max Magnitude | 0 |
[PMID 15832309] Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
