rs9727115
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9727115(A;A) |
Make rs9727115(A;G) |
Make rs9727115(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 98711697 |
Gene | SNX7 |
is a | snp |
is | mentioned by |
dbSNP | rs9727115 |
dbSNP (classic) | rs9727115 |
ClinGen | rs9727115 |
ebi | rs9727115 |
HLI | rs9727115 |
Exac | rs9727115 |
Gnomad | rs9727115 |
Varsome | rs9727115 |
LitVar | rs9727115 |
Map | rs9727115 |
PheGenI | rs9727115 |
Biobank | rs9727115 |
1000 genomes | rs9727115 |
hgdp | rs9727115 |
ensembl | rs9727115 |
geneview | rs9727115 |
scholar | rs9727115 |
rs9727115 | |
pharmgkb | rs9727115 |
gwascentral | rs9727115 |
openSNP | rs9727115 |
23andMe | rs9727115 |
SNPshot | rs9727115 |
SNPdbe | rs9727115 |
MSV3d | rs9727115 |
GWAS Ctlg | rs9727115 |
GMAF | 0.3691 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | G |
P-val | 2E-7 |
Odds Ratio | None None |