rs17679127
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs17679127(A;G) |
| Make rs17679127(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 103423754 |
| Gene | MARK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17679127 |
| dbSNP (classic) | rs17679127 |
| ClinGen | rs17679127 |
| ebi | rs17679127 |
| HLI | rs17679127 |
| Exac | rs17679127 |
| Gnomad | rs17679127 |
| Varsome | rs17679127 |
| LitVar | rs17679127 |
| Map | rs17679127 |
| PheGenI | rs17679127 |
| Biobank | rs17679127 |
| 1000 genomes | rs17679127 |
| hgdp | rs17679127 |
| ensembl | rs17679127 |
| geneview | rs17679127 |
| scholar | rs17679127 |
| rs17679127 | |
| pharmgkb | rs17679127 |
| gwascentral | rs17679127 |
| openSNP | rs17679127 |
| 23andMe | rs17679127 |
| SNPshot | rs17679127 |
| SNPdbe | rs17679127 |
| MSV3d | rs17679127 |
| GWAS Ctlg | rs17679127 |
| GMAF | 0.07484 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20697106
] Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32
