rs4148112
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs4148112(C;T) |
| Make rs4148112(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 21 |
| Position | 42230666 |
| Gene | ABCG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4148112 |
| dbSNP (classic) | rs4148112 |
| ClinGen | rs4148112 |
| ebi | rs4148112 |
| HLI | rs4148112 |
| Exac | rs4148112 |
| Gnomad | rs4148112 |
| Varsome | rs4148112 |
| LitVar | rs4148112 |
| Map | rs4148112 |
| PheGenI | rs4148112 |
| Biobank | rs4148112 |
| 1000 genomes | rs4148112 |
| hgdp | rs4148112 |
| ensembl | rs4148112 |
| geneview | rs4148112 |
| scholar | rs4148112 |
| rs4148112 | |
| pharmgkb | rs4148112 |
| gwascentral | rs4148112 |
| openSNP | rs4148112 |
| 23andMe | rs4148112 |
| SNPshot | rs4148112 |
| SNPdbe | rs4148112 |
| MSV3d | rs4148112 |
| GWAS Ctlg | rs4148112 |
| Max Magnitude | 0 |
| 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 | 5E-7 |
| Odds Ratio | NR NR |
