rs443198
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs443198(C;C) |
| Make rs443198(C;T) |
| Make rs443198(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32222629 |
| Gene | NOTCH4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs443198 |
| dbSNP (classic) | rs443198 |
| ClinGen | rs443198 |
| ebi | rs443198 |
| HLI | rs443198 |
| Exac | rs443198 |
| Gnomad | rs443198 |
| Varsome | rs443198 |
| LitVar | rs443198 |
| Map | rs443198 |
| PheGenI | rs443198 |
| Biobank | rs443198 |
| 1000 genomes | rs443198 |
| hgdp | rs443198 |
| ensembl | rs443198 |
| geneview | rs443198 |
| scholar | rs443198 |
| rs443198 | |
| pharmgkb | rs443198 |
| gwascentral | rs443198 |
| openSNP | rs443198 |
| 23andMe | rs443198 |
| SNPshot | rs443198 |
| SNPdbe | rs443198 |
| MSV3d | rs443198 |
| GWAS Ctlg | rs443198 |
| GMAF | 0.4233 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21779181 ]
|
| Trait | |
| Title | Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. |
| Risk Allele | |
| P-val | 9E-21 |
| Odds Ratio | 1.8200 [1.59-2.04] |
[PMID 27231971] NOTCH4 gene polymorphisms as potential risk factors for brain arteriovenous malformation development and hemorrhagic presentation.
[PMID 31838262] A Notch4 missense mutation is associated with susceptibility to tuberculosis in Chinese population.
