rs2071278
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2071278(C;C) |
| Make rs2071278(C;T) |
| Make rs2071278(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32197667 |
| Gene | NOTCH4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2071278 |
| dbSNP (classic) | rs2071278 |
| ClinGen | rs2071278 |
| ebi | rs2071278 |
| HLI | rs2071278 |
| Exac | rs2071278 |
| Gnomad | rs2071278 |
| Varsome | rs2071278 |
| LitVar | rs2071278 |
| Map | rs2071278 |
| PheGenI | rs2071278 |
| Biobank | rs2071278 |
| 1000 genomes | rs2071278 |
| hgdp | rs2071278 |
| ensembl | rs2071278 |
| geneview | rs2071278 |
| scholar | rs2071278 |
| rs2071278 | |
| pharmgkb | rs2071278 |
| gwascentral | rs2071278 |
| openSNP | rs2071278 |
| 23andMe | rs2071278 |
| SNPshot | rs2071278 |
| SNPdbe | rs2071278 |
| MSV3d | rs2071278 |
| GWAS Ctlg | rs2071278 |
| GMAF | 0.1162 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23028341 ]
|
| Trait | Complement C3 and C4 levels |
| Title | Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. |
| Risk Allele | G |
| P-val | 4E-72 |
| Odds Ratio | .13 [0.11-0.15] g/L decrease |
[PMID 15747258] A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.
