rs362277
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs362277(A;A) |
| Make rs362277(A;G) |
| Make rs362277(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 3217326 |
| Gene | HTT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs362277 |
| dbSNP (classic) | rs362277 |
| ClinGen | rs362277 |
| ebi | rs362277 |
| HLI | rs362277 |
| Exac | rs362277 |
| Gnomad | rs362277 |
| Varsome | rs362277 |
| LitVar | rs362277 |
| Map | rs362277 |
| PheGenI | rs362277 |
| Biobank | rs362277 |
| 1000 genomes | rs362277 |
| hgdp | rs362277 |
| ensembl | rs362277 |
| geneview | rs362277 |
| scholar | rs362277 |
| rs362277 | |
| pharmgkb | rs362277 |
| gwascentral | rs362277 |
| openSNP | rs362277 |
| 23andMe | rs362277 |
| SNPshot | rs362277 |
| SNPdbe | rs362277 |
| MSV3d | rs362277 |
| GWAS Ctlg | rs362277 |
| GMAF | 0.1869 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22134093] Polymorphisms and noncardioembolic stroke in three case-control studies [PMID 16391835] Late-onset and typical Huntington disease families from Crete have distinct genetic origins.
