rs1423096
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1423096(A;A) |
Make rs1423096(A;G) |
Make rs1423096(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 7674291 |
is a | snp |
is | mentioned by |
dbSNP | rs1423096 |
dbSNP (classic) | rs1423096 |
ClinGen | rs1423096 |
ebi | rs1423096 |
HLI | rs1423096 |
Exac | rs1423096 |
Gnomad | rs1423096 |
Varsome | rs1423096 |
LitVar | rs1423096 |
Map | rs1423096 |
PheGenI | rs1423096 |
Biobank | rs1423096 |
1000 genomes | rs1423096 |
hgdp | rs1423096 |
ensembl | rs1423096 |
geneview | rs1423096 |
scholar | rs1423096 |
rs1423096 | |
pharmgkb | rs1423096 |
gwascentral | rs1423096 |
openSNP | rs1423096 |
23andMe | rs1423096 |
SNPshot | rs1423096 |
SNPdbe | rs1423096 |
MSV3d | rs1423096 |
GWAS Ctlg | rs1423096 |
GMAF | 0.1074 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24123702] Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: A Mendelian randomization effect
[PMID 19074981] Association of variants in RETN with plasma resistin levels and diabetes-related traits in the Framingham Offspring Study.