rs778906552
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs778906552(A;A) |
| Make rs778906552(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 75734846 |
| Gene | ACADM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs778906552 |
| dbSNP (classic) | rs778906552 |
| ClinGen | rs778906552 |
| ebi | rs778906552 |
| HLI | rs778906552 |
| Exac | rs778906552 |
| Gnomad | rs778906552 |
| Varsome | rs778906552 |
| LitVar | rs778906552 |
| Map | rs778906552 |
| PheGenI | rs778906552 |
| Biobank | rs778906552 |
| 1000 genomes | rs778906552 |
| hgdp | rs778906552 |
| ensembl | rs778906552 |
| geneview | rs778906552 |
| scholar | rs778906552 |
| rs778906552 | |
| pharmgkb | rs778906552 |
| gwascentral | rs778906552 |
| openSNP | rs778906552 |
| 23andMe | rs778906552 |
| SNPshot | rs778906552 |
| SNPdbe | rs778906552 |
| MSV3d | rs778906552 |
| GWAS Ctlg | rs778906552 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs778906552(A;A) |
| Alt | rs778906552(A;A) |
| Reference | Rs778906552(G;G) |
| Significance | Other |
| Disease | not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency |
| Variation | info |
| Gene | ACADM |
| CLNDBN | not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency |
| Reversed | 0 |
| HGVS | NC_000001.10:g.76200531G>A |
| CLNSRC | |
| CLNACC | RCV000179231.4, RCV000211501.2, |
