rs1129740
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1129740(A;A) |
Make rs1129740(A;G) |
Make rs1129740(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 32641328 |
Gene | HLA-DQA1, LOC107986589 |
is a | snp |
is | mentioned by |
dbSNP | rs1129740 |
dbSNP (classic) | rs1129740 |
ClinGen | rs1129740 |
ebi | rs1129740 |
HLI | rs1129740 |
Exac | rs1129740 |
Gnomad | rs1129740 |
Varsome | rs1129740 |
LitVar | rs1129740 |
Map | rs1129740 |
PheGenI | rs1129740 |
Biobank | rs1129740 |
1000 genomes | rs1129740 |
hgdp | rs1129740 |
ensembl | rs1129740 |
geneview | rs1129740 |
scholar | rs1129740 |
rs1129740 | |
pharmgkb | rs1129740 |
gwascentral | rs1129740 |
openSNP | rs1129740 |
23andMe | rs1129740 |
SNPshot | rs1129740 |
SNPdbe | rs1129740 |
MSV3d | rs1129740 |
GWAS Ctlg | rs1129740 |
Max Magnitude | 0 |
Rs1129740 is a missense variant, C34Y, in HLA-DQA1.
It has been associated with Steroid-sensitive nephrotic syndrome (SSNS). [PMID 25349203]
[PMID 30006974] Association of HLA-DQA1 gene polymorphisms with the risk of children primary nephrotic syndrome in Chinese population.