rs4902359
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs4902359(A;A) |
| Make rs4902359(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 65076072 |
| Gene | MAX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4902359 |
| dbSNP (classic) | rs4902359 |
| ClinGen | rs4902359 |
| ebi | rs4902359 |
| HLI | rs4902359 |
| Exac | rs4902359 |
| Gnomad | rs4902359 |
| Varsome | rs4902359 |
| LitVar | rs4902359 |
| Map | rs4902359 |
| PheGenI | rs4902359 |
| Biobank | rs4902359 |
| 1000 genomes | rs4902359 |
| hgdp | rs4902359 |
| ensembl | rs4902359 |
| geneview | rs4902359 |
| scholar | rs4902359 |
| rs4902359 | |
| pharmgkb | rs4902359 |
| gwascentral | rs4902359 |
| openSNP | rs4902359 |
| 23andMe | rs4902359 |
| SNPshot | rs4902359 |
| SNPdbe | rs4902359 |
| MSV3d | rs4902359 |
| GWAS Ctlg | rs4902359 |
| GMAF | 0.4596 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23743562] MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours
| ClinVar | |
|---|---|
| Risk | rs4902359(A;A) |
| Alt | rs4902359(A;A) |
| Reference | Rs4902359(G;G) |
| Significance | Non-pathogenic |
| Disease | Pheochromocytoma |
| Variation | info |
| Gene | MAX |
| CLNDBN | Pheochromocytoma |
| Reversed | 0 |
| HGVS | NC_000014.8:g.65542790G>A |
| CLNSRC | |
| CLNACC | RCV000325472.1, |
