rs3129720
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3129720(C;C) |
| Make rs3129720(C;T) |
| Make rs3129720(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32695854 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3129720 |
| dbSNP (classic) | rs3129720 |
| ClinGen | rs3129720 |
| ebi | rs3129720 |
| HLI | rs3129720 |
| Exac | rs3129720 |
| Gnomad | rs3129720 |
| Varsome | rs3129720 |
| LitVar | rs3129720 |
| Map | rs3129720 |
| PheGenI | rs3129720 |
| Biobank | rs3129720 |
| 1000 genomes | rs3129720 |
| hgdp | rs3129720 |
| ensembl | rs3129720 |
| geneview | rs3129720 |
| scholar | rs3129720 |
| rs3129720 | |
| pharmgkb | rs3129720 |
| gwascentral | rs3129720 |
| openSNP | rs3129720 |
| 23andMe | rs3129720 |
| SNPshot | rs3129720 |
| SNPdbe | rs3129720 |
| MSV3d | rs3129720 |
| GWAS Ctlg | rs3129720 |
| GMAF | 0.2039 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22493691 ]
|
| Trait | |
| Title | Novel associations for hypothyroidism include known autoimmune risk loci. |
| Risk Allele | C |
| P-val | 5E-7 |
| Odds Ratio | 1.1600 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 23472185]
|
| Trait | Multiple sclerosis (OCB status) |
| Title | Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. |
| Risk Allele | |
| P-val | 5E-15 |
| Odds Ratio | 1.91 [1.62-2.24] |
