rs17000900
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17000900(A;A) |
| Make rs17000900(A;C) |
| Make rs17000900(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 41426103 |
| Gene | MX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17000900 |
| dbSNP (classic) | rs17000900 |
| ClinGen | rs17000900 |
| ebi | rs17000900 |
| HLI | rs17000900 |
| Exac | rs17000900 |
| Gnomad | rs17000900 |
| Varsome | rs17000900 |
| LitVar | rs17000900 |
| Map | rs17000900 |
| PheGenI | rs17000900 |
| Biobank | rs17000900 |
| 1000 genomes | rs17000900 |
| hgdp | rs17000900 |
| ensembl | rs17000900 |
| geneview | rs17000900 |
| scholar | rs17000900 |
| rs17000900 | |
| pharmgkb | rs17000900 |
| gwascentral | rs17000900 |
| openSNP | rs17000900 |
| 23andMe | rs17000900 |
| SNPshot | rs17000900 |
| SNPdbe | rs17000900 |
| MSV3d | rs17000900 |
| GWAS Ctlg | rs17000900 |
| GMAF | 0.1488 |
| Max Magnitude | 0 |
[PMID 23160781
] MxA transcripts with distinct first exons and modulation of gene expression levels by single-nucleotide polymorphisms in human bronchial epithelial cells
[PMID 17126411] Pharmacogenetics of MXA SNPs in interferon-beta treated multiple sclerosis patients.
[PMID 22950423] MxA polymorphisms are associated with risk and age-at-onset in Alzheimer disease and accelerated cognitive decline in Chinese elders.
