rs13100616
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13100616(A;A) |
| Make rs13100616(A;G) |
| Make rs13100616(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 178681763 |
| Gene | KCNMB2, KCNMB2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13100616 |
| dbSNP (classic) | rs13100616 |
| ClinGen | rs13100616 |
| ebi | rs13100616 |
| HLI | rs13100616 |
| Exac | rs13100616 |
| Gnomad | rs13100616 |
| Varsome | rs13100616 |
| LitVar | rs13100616 |
| Map | rs13100616 |
| PheGenI | rs13100616 |
| Biobank | rs13100616 |
| 1000 genomes | rs13100616 |
| hgdp | rs13100616 |
| ensembl | rs13100616 |
| geneview | rs13100616 |
| scholar | rs13100616 |
| rs13100616 | |
| pharmgkb | rs13100616 |
| gwascentral | rs13100616 |
| openSNP | rs13100616 |
| 23andMe | rs13100616 |
| SNPshot | rs13100616 |
| SNPdbe | rs13100616 |
| MSV3d | rs13100616 |
| GWAS Ctlg | rs13100616 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24529757] |
| Trait | Amyotrophic lateral sclerosis (sporadic) |
| Title | A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
| Risk Allele | |
| P-val | 9E-7 |
| Odds Ratio | NR NR |
