rs2278107
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2278107(C;C) |
| Make rs2278107(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 93410921 |
| Gene | EPHA7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2278107 |
| dbSNP (classic) | rs2278107 |
| ClinGen | rs2278107 |
| ebi | rs2278107 |
| HLI | rs2278107 |
| Exac | rs2278107 |
| Gnomad | rs2278107 |
| Varsome | rs2278107 |
| LitVar | rs2278107 |
| Map | rs2278107 |
| PheGenI | rs2278107 |
| Biobank | rs2278107 |
| 1000 genomes | rs2278107 |
| hgdp | rs2278107 |
| ensembl | rs2278107 |
| geneview | rs2278107 |
| scholar | rs2278107 |
| rs2278107 | |
| pharmgkb | rs2278107 |
| gwascentral | rs2278107 |
| openSNP | rs2278107 |
| 23andMe | rs2278107 |
| SNPshot | rs2278107 |
| SNPdbe | rs2278107 |
| MSV3d | rs2278107 |
| GWAS Ctlg | rs2278107 |
| GMAF | 0.06474 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
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[PMID 18853455
] Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.
