rs76208147
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs76208147(C;C) |
| Make rs76208147(C;T) |
| Make rs76208147(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 3 |
| Position | 47121396 |
| Gene | SETD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76208147 |
| dbSNP (classic) | rs76208147 |
| ClinGen | rs76208147 |
| ebi | rs76208147 |
| HLI | rs76208147 |
| Exac | rs76208147 |
| Gnomad | rs76208147 |
| Varsome | rs76208147 |
| LitVar | rs76208147 |
| Map | rs76208147 |
| PheGenI | rs76208147 |
| Biobank | rs76208147 |
| 1000 genomes | rs76208147 |
| hgdp | rs76208147 |
| ensembl | rs76208147 |
| geneview | rs76208147 |
| scholar | rs76208147 |
| rs76208147 | |
| pharmgkb | rs76208147 |
| gwascentral | rs76208147 |
| openSNP | rs76208147 |
| 23andMe | rs76208147 |
| SNPshot | rs76208147 |
| SNPdbe | rs76208147 |
| MSV3d | rs76208147 |
| GWAS Ctlg | rs76208147 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
| ClinVar | |
|---|---|
| Risk | rs76208147(T;T) |
| Alt | rs76208147(T;T) |
| Reference | rs76208147(C;C) |
| Significance | Untested |
| Disease | not specified |
| Variation | info |
| Gene | SETD2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000003.11:g.47162886C>T |
| CLNSRC | |
| CLNACC | RCV000122047.1, |
[PMID 30922329] Genetic polymorphisms of histone methyltransferase SETD2 predicts prognosis and chemotherapy response in Chinese acute myeloid leukemia patients.
