rs11551664
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs11551664(C;T) |
| Make rs11551664(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 19 |
| Position | 1390985 |
| Gene | NDUFS7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11551664 |
| dbSNP (classic) | rs11551664 |
| ClinGen | rs11551664 |
| ebi | rs11551664 |
| HLI | rs11551664 |
| Exac | rs11551664 |
| Gnomad | rs11551664 |
| Varsome | rs11551664 |
| LitVar | rs11551664 |
| Map | rs11551664 |
| PheGenI | rs11551664 |
| Biobank | rs11551664 |
| 1000 genomes | rs11551664 |
| hgdp | rs11551664 |
| ensembl | rs11551664 |
| geneview | rs11551664 |
| scholar | rs11551664 |
| rs11551664 | |
| pharmgkb | rs11551664 |
| gwascentral | rs11551664 |
| openSNP | rs11551664 |
| 23andMe | rs11551664 |
| SNPshot | rs11551664 |
| SNPdbe | rs11551664 |
| MSV3d | rs11551664 |
| GWAS Ctlg | rs11551664 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs11551664(T;T) |
| Alt | rs11551664(T;T) |
| Reference | Rs11551664(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | NDUFS7 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.1390984C>T |
| CLNSRC | |
| CLNACC | RCV000195624.2, |
