rs10838681
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10838681(A;A) |
Make rs10838681(A;G) |
Make rs10838681(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 47253513 |
Gene | NR1H3 |
is a | snp |
is | mentioned by |
dbSNP | rs10838681 |
dbSNP (classic) | rs10838681 |
ClinGen | rs10838681 |
ebi | rs10838681 |
HLI | rs10838681 |
Exac | rs10838681 |
Gnomad | rs10838681 |
Varsome | rs10838681 |
LitVar | rs10838681 |
Map | rs10838681 |
PheGenI | rs10838681 |
Biobank | rs10838681 |
1000 genomes | rs10838681 |
hgdp | rs10838681 |
ensembl | rs10838681 |
geneview | rs10838681 |
scholar | rs10838681 |
rs10838681 | |
pharmgkb | rs10838681 |
gwascentral | rs10838681 |
openSNP | rs10838681 |
23andMe | rs10838681 |
SNPshot | rs10838681 |
SNPdbe | rs10838681 |
MSV3d | rs10838681 |
GWAS Ctlg | rs10838681 |
GMAF | 0.4284 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22399527![]() |
Trait | |
Title | Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. |
Risk Allele | G |
P-val | 1E-9 |
Odds Ratio | 0.0800 None |
[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.