rs779626155
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs779626155(A;A) |
| Make rs779626155(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 25240313 |
| Gene | DNMT3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs779626155 |
| dbSNP (classic) | rs779626155 |
| ClinGen | rs779626155 |
| ebi | rs779626155 |
| HLI | rs779626155 |
| Exac | rs779626155 |
| Gnomad | rs779626155 |
| Varsome | rs779626155 |
| LitVar | rs779626155 |
| Map | rs779626155 |
| PheGenI | rs779626155 |
| Biobank | rs779626155 |
| 1000 genomes | rs779626155 |
| hgdp | rs779626155 |
| ensembl | rs779626155 |
| geneview | rs779626155 |
| scholar | rs779626155 |
| rs779626155 | |
| pharmgkb | rs779626155 |
| gwascentral | rs779626155 |
| openSNP | rs779626155 |
| 23andMe | rs779626155 |
| SNPshot | rs779626155 |
| SNPdbe | rs779626155 |
| MSV3d | rs779626155 |
| GWAS Ctlg | rs779626155 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs779626155(A;A) |
| Alt | rs779626155(A;A) |
| Reference | Rs779626155(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DNMT3A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.25463182G>A |
| CLNSRC | |
| CLNACC | RCV000486209.1, |
