Difference between revisions of "Rs3093662"
From SNPedia
(Update Rsnum - Set: Chromosome Orientation geno1 geno2 geno3 Gene position Assembly GenomeBuild dbSNPBuild) |
(Update population template to HapMap release 27) |
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| Line 11: | Line 11: | ||
|GenomeBuild=37.1 | |GenomeBuild=37.1 | ||
|dbSNPBuild=131 | |dbSNPBuild=131 | ||
| + | }}{{ population diversity | ||
| + | | geno1=(A;A) | ||
| + | | geno2=(A;G) | ||
| + | | geno3=(G;G) | ||
| + | | CEU | 85.0 | 15.0 | 0.0 | ||
| + | | HCB | 94.0 | 4.8 | 1.2 | ||
| + | | JPT | 95.3 | 4.7 | 0.0 | ||
| + | | YRI | 88.5 | 10.6 | 0.9 | ||
| + | | ASW | 81.1 | 18.9 | 0.0 | ||
| + | | CHB | 94.0 | 4.8 | 1.2 | ||
| + | | CHD | 95.3 | 4.7 | 0.0 | ||
| + | | GIH | 68.2 | 30.7 | 1.1 | ||
| + | | LWK | 82.2 | 17.8 | 0.0 | ||
| + | | MEX | 78.0 | 20.0 | 2.0 | ||
| + | | MKK | 65.0 | 33.6 | 1.4 | ||
| + | | TSI | 79.5 | 19.3 | 1.1 | ||
| + | | HapMapRevision=27 | ||
}}{{PMID Auto | }}{{PMID Auto | ||
|PMID=20459604 | |PMID=20459604 | ||
Revision as of 07:06, 28 June 2010
| Orientation | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs3093662(A;G) |
| Make rs3093662(G;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 6 |
| Position | 31544189 |
| Gene | TNF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3093662 |
| dbSNP (classic) | rs3093662 |
| ClinGen | rs3093662 |
| ebi | rs3093662 |
| HLI | rs3093662 |
| Exac | rs3093662 |
| Gnomad | rs3093662 |
| Varsome | rs3093662 |
| LitVar | rs3093662 |
| Map | rs3093662 |
| PheGenI | rs3093662 |
| Biobank | rs3093662 |
| 1000 genomes | rs3093662 |
| hgdp | rs3093662 |
| ensembl | rs3093662 |
| geneview | rs3093662 |
| scholar | rs3093662 |
| rs3093662 | |
| pharmgkb | rs3093662 |
| gwascentral | rs3093662 |
| openSNP | rs3093662 |
| 23andMe | rs3093662 |
| SNPshot | rs3093662 |
| SNPdbe | rs3093662 |
| MSV3d | rs3093662 |
| GWAS Ctlg | rs3093662 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 27 |
|---|---|---|
|
| ||
[PMID 20459604] Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes
