rs920946076
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 25247160 |
| Gene | DNMT3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs920946076 |
| dbSNP (classic) | rs920946076 |
| ClinGen | rs920946076 |
| ebi | rs920946076 |
| HLI | rs920946076 |
| Exac | rs920946076 |
| Gnomad | rs920946076 |
| Varsome | rs920946076 |
| LitVar | rs920946076 |
| Map | rs920946076 |
| PheGenI | rs920946076 |
| Biobank | rs920946076 |
| 1000 genomes | rs920946076 |
| hgdp | rs920946076 |
| ensembl | rs920946076 |
| geneview | rs920946076 |
| scholar | rs920946076 |
| rs920946076 | |
| pharmgkb | rs920946076 |
| gwascentral | rs920946076 |
| openSNP | rs920946076 |
| 23andMe | rs920946076 |
| SNPshot | rs920946076 |
| SNPdbe | rs920946076 |
| MSV3d | rs920946076 |
| GWAS Ctlg | rs920946076 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs920946076(C;C) |
| Alt | rs920946076(C;C) |
| Reference | Rs920946076(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DNMT3A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.25470029T>C |
| CLNSRC | |
| CLNACC | RCV000481026.1, |
