rs747593459
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs747593459(G;G) |
| Make rs747593459(G;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 75750527 |
| Gene | ACADM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs747593459 |
| dbSNP (classic) | rs747593459 |
| ClinGen | rs747593459 |
| ebi | rs747593459 |
| HLI | rs747593459 |
| Exac | rs747593459 |
| Gnomad | rs747593459 |
| Varsome | rs747593459 |
| LitVar | rs747593459 |
| Map | rs747593459 |
| PheGenI | rs747593459 |
| Biobank | rs747593459 |
| 1000 genomes | rs747593459 |
| hgdp | rs747593459 |
| ensembl | rs747593459 |
| geneview | rs747593459 |
| scholar | rs747593459 |
| rs747593459 | |
| pharmgkb | rs747593459 |
| gwascentral | rs747593459 |
| openSNP | rs747593459 |
| 23andMe | rs747593459 |
| SNPshot | rs747593459 |
| SNPdbe | rs747593459 |
| MSV3d | rs747593459 |
| GWAS Ctlg | rs747593459 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs747593459(G;G) |
| Alt | rs747593459(G;G) |
| Reference | Rs747593459(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ACADM |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.76216212T>G |
| CLNSRC | |
| CLNACC | RCV000185678.1, |
