rs7072398
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7072398(A;A) |
| Make rs7072398(A;G) |
| Make rs7072398(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 6037883 |
| Gene | IL2RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7072398 |
| dbSNP (classic) | rs7072398 |
| ClinGen | rs7072398 |
| ebi | rs7072398 |
| HLI | rs7072398 |
| Exac | rs7072398 |
| Gnomad | rs7072398 |
| Varsome | rs7072398 |
| LitVar | rs7072398 |
| Map | rs7072398 |
| PheGenI | rs7072398 |
| Biobank | rs7072398 |
| 1000 genomes | rs7072398 |
| hgdp | rs7072398 |
| ensembl | rs7072398 |
| geneview | rs7072398 |
| scholar | rs7072398 |
| rs7072398 | |
| pharmgkb | rs7072398 |
| gwascentral | rs7072398 |
| openSNP | rs7072398 |
| 23andMe | rs7072398 |
| SNPshot | rs7072398 |
| SNPdbe | rs7072398 |
| MSV3d | rs7072398 |
| GWAS Ctlg | rs7072398 |
| GMAF | 0.4793 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| Rs7072398 | |
|---|---|
| PubMed | [PMID 17371467] |
| Affy Probeset | SNP_A-4246476 |
| Affy Orientation | reverse |
| On GW 5.0 | 0 |
| Alleles A/B | C/T |
| Ancestral | G |
| Population | UK |
| Allele | |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.09 |
| Disease | Graves' Disease (GD) |
[PMID 16400611
] Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
[PMID 19956101
] Overview of the Rapid Response data.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- Has Report GE
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
