rs422951
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs422951(A;A) |
| Make rs422951(A;G) |
| Make rs422951(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32220606 |
| Gene | NOTCH4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs422951 |
| dbSNP (classic) | rs422951 |
| ClinGen | rs422951 |
| ebi | rs422951 |
| HLI | rs422951 |
| Exac | rs422951 |
| Gnomad | rs422951 |
| Varsome | rs422951 |
| LitVar | rs422951 |
| Map | rs422951 |
| PheGenI | rs422951 |
| Biobank | rs422951 |
| 1000 genomes | rs422951 |
| hgdp | rs422951 |
| ensembl | rs422951 |
| geneview | rs422951 |
| scholar | rs422951 |
| rs422951 | |
| pharmgkb | rs422951 |
| gwascentral | rs422951 |
| openSNP | rs422951 |
| 23andMe | rs422951 |
| SNPshot | rs422951 |
| SNPdbe | rs422951 |
| MSV3d | rs422951 |
| GWAS Ctlg | rs422951 |
| GMAF | 0.3347 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22732452] Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis
[PMID 15091315] Is NOTCH4 associated with schizophrenia?
[PMID 23549433] A NOTCH4 missense mutation confers resistance to multiple sclerosis in Japanese.
[PMID 25802187] Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
[PMID 28568708
] Prognostic value of Notch receptors in postsurgical patients with hepatitis B virus-related hepatocellular carcinoma.
[PMID 31838262] A Notch4 missense mutation is associated with susceptibility to tuberculosis in Chinese population.
