rs868213
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs868213(C;C) |
| Make rs868213(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 67186554 |
| Gene | EXOC3L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs868213 |
| dbSNP (classic) | rs868213 |
| ClinGen | rs868213 |
| ebi | rs868213 |
| HLI | rs868213 |
| Exac | rs868213 |
| Gnomad | rs868213 |
| Varsome | rs868213 |
| LitVar | rs868213 |
| Map | rs868213 |
| PheGenI | rs868213 |
| Biobank | rs868213 |
| 1000 genomes | rs868213 |
| hgdp | rs868213 |
| ensembl | rs868213 |
| geneview | rs868213 |
| scholar | rs868213 |
| rs868213 | |
| pharmgkb | rs868213 |
| gwascentral | rs868213 |
| openSNP | rs868213 |
| 23andMe | rs868213 |
| SNPshot | rs868213 |
| SNPdbe | rs868213 |
| MSV3d | rs868213 |
| GWAS Ctlg | rs868213 |
| GMAF | 0.1492 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19854717
] The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)
23andMe reports that each G allele at rs868213 appears to be associated with 1.5x higher odds of ankylosing spondylitis. [PMID 19854717]
