rs2466293
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2466293(C;C) |
Make rs2466293(C;T) |
Make rs2466293(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 117173699 |
Gene | LOC105375716, SLC30A8 |
is a | snp |
is | mentioned by |
dbSNP | rs2466293 |
dbSNP (classic) | rs2466293 |
ClinGen | rs2466293 |
ebi | rs2466293 |
HLI | rs2466293 |
Exac | rs2466293 |
Gnomad | rs2466293 |
Varsome | rs2466293 |
LitVar | rs2466293 |
Map | rs2466293 |
PheGenI | rs2466293 |
Biobank | rs2466293 |
1000 genomes | rs2466293 |
hgdp | rs2466293 |
ensembl | rs2466293 |
geneview | rs2466293 |
scholar | rs2466293 |
rs2466293 | |
pharmgkb | rs2466293 |
gwascentral | rs2466293 |
openSNP | rs2466293 |
23andMe | rs2466293 |
SNPshot | rs2466293 |
SNPdbe | rs2466293 |
MSV3d | rs2466293 |
GWAS Ctlg | rs2466293 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26109524] Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese