rs2071277
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2071277(A;A) |
| Make rs2071277(A;G) |
| Make rs2071277(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32203906 |
| Gene | NOTCH4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2071277 |
| dbSNP (classic) | rs2071277 |
| ClinGen | rs2071277 |
| ebi | rs2071277 |
| HLI | rs2071277 |
| Exac | rs2071277 |
| Gnomad | rs2071277 |
| Varsome | rs2071277 |
| LitVar | rs2071277 |
| Map | rs2071277 |
| PheGenI | rs2071277 |
| Biobank | rs2071277 |
| 1000 genomes | rs2071277 |
| hgdp | rs2071277 |
| ensembl | rs2071277 |
| geneview | rs2071277 |
| scholar | rs2071277 |
| rs2071277 | |
| pharmgkb | rs2071277 |
| gwascentral | rs2071277 |
| openSNP | rs2071277 |
| 23andMe | rs2071277 |
| SNPshot | rs2071277 |
| SNPdbe | rs2071277 |
| MSV3d | rs2071277 |
| GWAS Ctlg | rs2071277 |
| GMAF | 0.4215 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22694956 ]
|
| Trait | |
| Title | Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. |
| Risk Allele | C |
| P-val | 2E-11 |
| Odds Ratio | 1.3000 None |
[PMID 31838262] A Notch4 missense mutation is associated with susceptibility to tuberculosis in Chinese population.
