rs149095705
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs149095705(A;A) |
| Make rs149095705(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 25234307 |
| Gene | DNMT3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149095705 |
| dbSNP (classic) | rs149095705 |
| ClinGen | rs149095705 |
| ebi | rs149095705 |
| HLI | rs149095705 |
| Exac | rs149095705 |
| Gnomad | rs149095705 |
| Varsome | rs149095705 |
| LitVar | rs149095705 |
| Map | rs149095705 |
| PheGenI | rs149095705 |
| Biobank | rs149095705 |
| 1000 genomes | rs149095705 |
| hgdp | rs149095705 |
| ensembl | rs149095705 |
| geneview | rs149095705 |
| scholar | rs149095705 |
| rs149095705 | |
| pharmgkb | rs149095705 |
| gwascentral | rs149095705 |
| openSNP | rs149095705 |
| 23andMe | rs149095705 |
| SNPshot | rs149095705 |
| SNPdbe | rs149095705 |
| MSV3d | rs149095705 |
| GWAS Ctlg | rs149095705 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149095705(A;A) rs149095705(C;C) rs149095705(T;T) |
| Alt | rs149095705(A;A) rs149095705(C;C) rs149095705(T;T) |
| Reference | Rs149095705(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DNMT3A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.25457176G>A |
| CLNSRC | |
| CLNACC | RCV000413992.1, |
