rs5472909
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs5472909(C;C) |
Make rs5472909(C;G) |
Make rs5472909(G;G) |
Reference | AgamP3 3.1/137 |
Chromosome | 3L |
Position | 24137765 |
is a | snp |
is | mentioned by |
dbSNP | rs5472909 |
dbSNP (classic) | rs5472909 |
ClinGen | rs5472909 |
ebi | rs5472909 |
HLI | rs5472909 |
Exac | rs5472909 |
Gnomad | rs5472909 |
Varsome | rs5472909 |
LitVar | rs5472909 |
Map | rs5472909 |
PheGenI | rs5472909 |
Biobank | rs5472909 |
1000 genomes | rs5472909 |
hgdp | rs5472909 |
ensembl | rs5472909 |
geneview | rs5472909 |
scholar | rs5472909 |
rs5472909 | |
pharmgkb | rs5472909 |
gwascentral | rs5472909 |
openSNP | rs5472909 |
23andMe | rs5472909 |
SNPshot | rs5472909 |
SNPdbe | rs5472909 |
MSV3d | rs5472909 |
GWAS Ctlg | rs5472909 |
Max Magnitude | 0 |
[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease