rs4790333
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4790333(C;C) |
Make rs4790333(C;T) |
Make rs4790333(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 2359409 |
Gene | SGSM2 |
is a | snp |
is | mentioned by |
dbSNP | rs4790333 |
dbSNP (classic) | rs4790333 |
ClinGen | rs4790333 |
ebi | rs4790333 |
HLI | rs4790333 |
Exac | rs4790333 |
Gnomad | rs4790333 |
Varsome | rs4790333 |
LitVar | rs4790333 |
Map | rs4790333 |
PheGenI | rs4790333 |
Biobank | rs4790333 |
1000 genomes | rs4790333 |
hgdp | rs4790333 |
ensembl | rs4790333 |
geneview | rs4790333 |
scholar | rs4790333 |
rs4790333 | |
pharmgkb | rs4790333 |
gwascentral | rs4790333 |
openSNP | rs4790333 |
23andMe | rs4790333 |
SNPshot | rs4790333 |
SNPdbe | rs4790333 |
MSV3d | rs4790333 |
GWAS Ctlg | rs4790333 |
GMAF | 0.4835 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21873549![]() |
Trait | |
Title | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. |
Risk Allele | T |
P-val | 3E-9 |
Odds Ratio | None None |