rs12753193
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12753193(A;A) |
Make rs12753193(A;G) |
Make rs12753193(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 65703996 |
is a | snp |
is | mentioned by |
dbSNP | rs12753193 |
dbSNP (classic) | rs12753193 |
ClinGen | rs12753193 |
ebi | rs12753193 |
HLI | rs12753193 |
Exac | rs12753193 |
Gnomad | rs12753193 |
Varsome | rs12753193 |
LitVar | rs12753193 |
Map | rs12753193 |
PheGenI | rs12753193 |
Biobank | rs12753193 |
1000 genomes | rs12753193 |
hgdp | rs12753193 |
ensembl | rs12753193 |
geneview | rs12753193 |
scholar | rs12753193 |
rs12753193 | |
pharmgkb | rs12753193 |
gwascentral | rs12753193 |
openSNP | rs12753193 |
23andMe | rs12753193 |
SNPshot | rs12753193 |
SNPdbe | rs12753193 |
MSV3d | rs12753193 |
GWAS Ctlg | rs12753193 |
GMAF | 0.4541 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19060910] |
Trait | Other metabolic traits |
Title | Genome-wide association analysis of metabolic traits in a birth cohort from a founder population |
Risk Allele | G |
P-val | 4E-7 |
Odds Ratio | 0.13 [-0.02-0.27] mmol/l decrease |
[PMID 20585554] On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study
[PMID 18439548] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
[PMID 18439552] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.