rs11906160
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11906160(A;A) |
Make rs11906160(A;G) |
Make rs11906160(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 34977952 |
Gene | MYH7B |
is a | snp |
is | mentioned by |
dbSNP | rs11906160 |
dbSNP (classic) | rs11906160 |
ClinGen | rs11906160 |
ebi | rs11906160 |
HLI | rs11906160 |
Exac | rs11906160 |
Gnomad | rs11906160 |
Varsome | rs11906160 |
LitVar | rs11906160 |
Map | rs11906160 |
PheGenI | rs11906160 |
Biobank | rs11906160 |
1000 genomes | rs11906160 |
hgdp | rs11906160 |
ensembl | rs11906160 |
geneview | rs11906160 |
scholar | rs11906160 |
rs11906160 | |
pharmgkb | rs11906160 |
gwascentral | rs11906160 |
openSNP | rs11906160 |
23andMe | rs11906160 |
SNPshot | rs11906160 |
SNPdbe | rs11906160 |
MSV3d | rs11906160 |
GWAS Ctlg | rs11906160 |
GMAF | 0.1423 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22216198] |
Trait | |
Title | A genome-wide association study of the Protein C anticoagulant pathway. |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | None None |