rs11256313
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11256313(A;A) |
Make rs11256313(A;G) |
Make rs11256313(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 6008329 |
is a | snp |
is | mentioned by |
dbSNP | rs11256313 |
dbSNP (classic) | rs11256313 |
ClinGen | rs11256313 |
ebi | rs11256313 |
HLI | rs11256313 |
Exac | rs11256313 |
Gnomad | rs11256313 |
Varsome | rs11256313 |
LitVar | rs11256313 |
Map | rs11256313 |
PheGenI | rs11256313 |
Biobank | rs11256313 |
1000 genomes | rs11256313 |
hgdp | rs11256313 |
ensembl | rs11256313 |
geneview | rs11256313 |
scholar | rs11256313 |
rs11256313 | |
pharmgkb | rs11256313 |
gwascentral | rs11256313 |
openSNP | rs11256313 |
23andMe | rs11256313 |
SNPshot | rs11256313 |
SNPdbe | rs11256313 |
MSV3d | rs11256313 |
GWAS Ctlg | rs11256313 |
GMAF | 0.1382 |
Max Magnitude | 0 |
[PMID 23170961] Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population