rs4958881
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common/normal |
| Make rs4958881(C;C) |
| Make rs4958881(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 151070675 |
| Gene | TNIP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4958881 |
| dbSNP (classic) | rs4958881 |
| ClinGen | rs4958881 |
| ebi | rs4958881 |
| HLI | rs4958881 |
| Exac | rs4958881 |
| Gnomad | rs4958881 |
| Varsome | rs4958881 |
| LitVar | rs4958881 |
| Map | rs4958881 |
| PheGenI | rs4958881 |
| Biobank | rs4958881 |
| 1000 genomes | rs4958881 |
| hgdp | rs4958881 |
| ensembl | rs4958881 |
| geneview | rs4958881 |
| scholar | rs4958881 |
| rs4958881 | |
| pharmgkb | rs4958881 |
| gwascentral | rs4958881 |
| openSNP | rs4958881 |
| 23andMe | rs4958881 |
| SNPshot | rs4958881 |
| SNPdbe | rs4958881 |
| MSV3d | rs4958881 |
| GWAS Ctlg | rs4958881 |
| GMAF | 0.1938 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22896740
] Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
| GWAS snp | |
|---|---|
| PMID | [PMID 23055271]
|
| Trait | Myasthenia gravis |
| Title | Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. |
| Risk Allele | G |
| P-val | 3E-10 |
| Odds Ratio | 1.73 [1.46-2.06] |
