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