rs742710
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs742710(A;A) |
| Make rs742710(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 5923382 |
| Gene | CHGB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs742710 |
| dbSNP (classic) | rs742710 |
| ClinGen | rs742710 |
| ebi | rs742710 |
| HLI | rs742710 |
| Exac | rs742710 |
| Gnomad | rs742710 |
| Varsome | rs742710 |
| LitVar | rs742710 |
| Map | rs742710 |
| PheGenI | rs742710 |
| Biobank | rs742710 |
| 1000 genomes | rs742710 |
| hgdp | rs742710 |
| ensembl | rs742710 |
| geneview | rs742710 |
| scholar | rs742710 |
| rs742710 | |
| pharmgkb | rs742710 |
| gwascentral | rs742710 |
| openSNP | rs742710 |
| 23andMe | rs742710 |
| SNPshot | rs742710 |
| SNPdbe | rs742710 |
| MSV3d | rs742710 |
| GWAS Ctlg | rs742710 |
| GMAF | 0.1455 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
23andMe blog 2x risk of ALS
[PMID 20007371
] Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
[PMID 20932227] The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.
