rs2070788
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2070788(C;C) |
| Make rs2070788(C;T) |
| Make rs2070788(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 21 |
| Position | 41470061 |
| Gene | TMPRSS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2070788 |
| dbSNP (classic) | rs2070788 |
| ClinGen | rs2070788 |
| ebi | rs2070788 |
| HLI | rs2070788 |
| Exac | rs2070788 |
| Gnomad | rs2070788 |
| Varsome | rs2070788 |
| LitVar | rs2070788 |
| Map | rs2070788 |
| PheGenI | rs2070788 |
| Biobank | rs2070788 |
| 1000 genomes | rs2070788 |
| hgdp | rs2070788 |
| ensembl | rs2070788 |
| geneview | rs2070788 |
| scholar | rs2070788 |
| rs2070788 | |
| pharmgkb | rs2070788 |
| gwascentral | rs2070788 |
| openSNP | rs2070788 |
| 23andMe | rs2070788 |
| SNPshot | rs2070788 |
| SNPdbe | rs2070788 |
| MSV3d | rs2070788 |
| GWAS Ctlg | rs2070788 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25904605
] The identification of TMPRSS2 as the susceptible gene for severe illness of 2009 pandemic A(H1N1) influenza and infection of A(H7N9) influenza:The GG genotype of rs2070788, a higher-expression variant of TMPRSS2, was a risk variant (odds ratio, 2.11; 95% confidence interval, 1.18-3.77; P = .01) to severe A(H1N1)pdm09 influenza.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 21
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
