rs12772169
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12772169(C;C) |
Make rs12772169(C;T) |
Make rs12772169(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94645572 |
Gene | LOC100130970 |
is a | snp |
is | mentioned by |
dbSNP | rs12772169 |
dbSNP (classic) | rs12772169 |
ClinGen | rs12772169 |
ebi | rs12772169 |
HLI | rs12772169 |
Exac | rs12772169 |
Gnomad | rs12772169 |
Varsome | rs12772169 |
LitVar | rs12772169 |
Map | rs12772169 |
PheGenI | rs12772169 |
Biobank | rs12772169 |
1000 genomes | rs12772169 |
hgdp | rs12772169 |
ensembl | rs12772169 |
geneview | rs12772169 |
scholar | rs12772169 |
rs12772169 | |
pharmgkb | rs12772169 |
gwascentral | rs12772169 |
openSNP | rs12772169 |
23andMe | rs12772169 |
SNPshot | rs12772169 |
SNPdbe | rs12772169 |
MSV3d | rs12772169 |
GWAS Ctlg | rs12772169 |
GMAF | 0.2934 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19578179] |
Trait | Acenocoumarol maintenance dosage |
Title | A genome-wide association study of acenocoumarol maintenance dosage |
Risk Allele | |
P-val | 8E-12 |
Odds Ratio | NR NR |
[PMID 23089684] Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates.
[PMID 28280103] Association of genetic variant and platelet function in patients undergoing neuroendovascular stenting.