rs4998557
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4998557(A;A) |
| Make rs4998557(A;G) |
| Make rs4998557(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 31662579 |
| Gene | SOD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4998557 |
| dbSNP (classic) | rs4998557 |
| ClinGen | rs4998557 |
| ebi | rs4998557 |
| HLI | rs4998557 |
| Exac | rs4998557 |
| Gnomad | rs4998557 |
| Varsome | rs4998557 |
| LitVar | rs4998557 |
| Map | rs4998557 |
| PheGenI | rs4998557 |
| Biobank | rs4998557 |
| 1000 genomes | rs4998557 |
| hgdp | rs4998557 |
| ensembl | rs4998557 |
| geneview | rs4998557 |
| scholar | rs4998557 |
| rs4998557 | |
| pharmgkb | rs4998557 |
| gwascentral | rs4998557 |
| openSNP | rs4998557 |
| 23andMe | rs4998557 |
| SNPshot | rs4998557 |
| SNPdbe | rs4998557 |
| MSV3d | rs4998557 |
| GWAS Ctlg | rs4998557 |
| GMAF | 0.3113 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22357533] [Association between SNPs in SOD1 and noise-induced hearing loss in Chinese Han population]
[PMID 18937358
] Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals.
[PMID 19306335] Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
[PMID 20872977] Mn-SOD and CuZn-SOD polymorphisms and interactions with risk factors in gastric cancer.
