rs17037621
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17037621(A;A) |
Make rs17037621(A;T) |
Make rs17037621(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 88606202 |
Gene | EIF2AK3 |
is a | snp |
is | mentioned by |
dbSNP | rs17037621 |
dbSNP (classic) | rs17037621 |
ClinGen | rs17037621 |
ebi | rs17037621 |
HLI | rs17037621 |
Exac | rs17037621 |
Gnomad | rs17037621 |
Varsome | rs17037621 |
LitVar | rs17037621 |
Map | rs17037621 |
PheGenI | rs17037621 |
Biobank | rs17037621 |
1000 genomes | rs17037621 |
hgdp | rs17037621 |
ensembl | rs17037621 |
geneview | rs17037621 |
scholar | rs17037621 |
rs17037621 | |
pharmgkb | rs17037621 |
gwascentral | rs17037621 |
openSNP | rs17037621 |
23andMe | rs17037621 |
SNPshot | rs17037621 |
SNPdbe | rs17037621 |
MSV3d | rs17037621 |
GWAS Ctlg | rs17037621 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24985580] Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population