rs1549318
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1549318(C;C) |
Make rs1549318(C;T) |
Make rs1549318(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 70816808 |
is a | snp |
is | mentioned by |
dbSNP | rs1549318 |
dbSNP (classic) | rs1549318 |
ClinGen | rs1549318 |
ebi | rs1549318 |
HLI | rs1549318 |
Exac | rs1549318 |
Gnomad | rs1549318 |
Varsome | rs1549318 |
LitVar | rs1549318 |
Map | rs1549318 |
PheGenI | rs1549318 |
Biobank | rs1549318 |
1000 genomes | rs1549318 |
hgdp | rs1549318 |
ensembl | rs1549318 |
geneview | rs1549318 |
scholar | rs1549318 |
rs1549318 | |
pharmgkb | rs1549318 |
gwascentral | rs1549318 |
openSNP | rs1549318 |
23andMe | rs1549318 |
SNPshot | rs1549318 |
SNPdbe | rs1549318 |
MSV3d | rs1549318 |
GWAS Ctlg | rs1549318 |
GMAF | 0.455 |
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 | 2E-10 |
Odds Ratio | None None |