rs7762619
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs7762619(G;G) |
| Make rs7762619(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31563533 |
| Gene | LOC100287329, LTA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7762619 |
| dbSNP (classic) | rs7762619 |
| ClinGen | rs7762619 |
| ebi | rs7762619 |
| HLI | rs7762619 |
| Exac | rs7762619 |
| Gnomad | rs7762619 |
| Varsome | rs7762619 |
| LitVar | rs7762619 |
| Map | rs7762619 |
| PheGenI | rs7762619 |
| Biobank | rs7762619 |
| 1000 genomes | rs7762619 |
| hgdp | rs7762619 |
| ensembl | rs7762619 |
| geneview | rs7762619 |
| scholar | rs7762619 |
| rs7762619 | |
| pharmgkb | rs7762619 |
| gwascentral | rs7762619 |
| openSNP | rs7762619 |
| 23andMe | rs7762619 |
| SNPshot | rs7762619 |
| SNPdbe | rs7762619 |
| MSV3d | rs7762619 |
| GWAS Ctlg | rs7762619 |
| GMAF | 0.01194 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20054343
] Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes
[PMID 19143814] Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1.
