rs876657565
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs876657565(C;T) |
| Make rs876657565(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 3396583 |
| Gene | PRDM16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876657565 |
| dbSNP (classic) | rs876657565 |
| ClinGen | rs876657565 |
| ebi | rs876657565 |
| HLI | rs876657565 |
| Exac | rs876657565 |
| Gnomad | rs876657565 |
| Varsome | rs876657565 |
| LitVar | rs876657565 |
| Map | rs876657565 |
| PheGenI | rs876657565 |
| Biobank | rs876657565 |
| 1000 genomes | rs876657565 |
| hgdp | rs876657565 |
| ensembl | rs876657565 |
| geneview | rs876657565 |
| scholar | rs876657565 |
| rs876657565 | |
| pharmgkb | rs876657565 |
| gwascentral | rs876657565 |
| openSNP | rs876657565 |
| 23andMe | rs876657565 |
| SNPshot | rs876657565 |
| SNPdbe | rs876657565 |
| MSV3d | rs876657565 |
| GWAS Ctlg | rs876657565 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876657565(T;T) |
| Alt | rs876657565(T;T) |
| Reference | Rs876657565(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | PRDM16 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000001.10:g.3313147C>T |
| CLNSRC | |
| CLNACC | RCV000488452.1, |
