rs536477
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs536477(A;A) |
Make rs536477(A;G) |
Make rs536477(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 239882608 |
Gene | CHRM3 |
is a | snp |
is | mentioned by |
dbSNP | rs536477 |
dbSNP (classic) | rs536477 |
ClinGen | rs536477 |
ebi | rs536477 |
HLI | rs536477 |
Exac | rs536477 |
Gnomad | rs536477 |
Varsome | rs536477 |
LitVar | rs536477 |
Map | rs536477 |
PheGenI | rs536477 |
Biobank | rs536477 |
1000 genomes | rs536477 |
hgdp | rs536477 |
ensembl | rs536477 |
geneview | rs536477 |
scholar | rs536477 |
rs536477 | |
pharmgkb | rs536477 |
gwascentral | rs536477 |
openSNP | rs536477 |
23andMe | rs536477 |
SNPshot | rs536477 |
SNPdbe | rs536477 |
MSV3d | rs536477 |
GWAS Ctlg | rs536477 |
GMAF | 0.4757 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23509962] |
Trait | Venous thromboembolism (gene x gene interaction) |
Title | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
Risk Allele | |
P-val | 3E-9 |
Odds Ratio | 1.59 [NR] |