rs1042194
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1042194(G;G) |
Make rs1042194(G;T) |
Make rs1042194(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 94735727 |
Gene | CYP2C18 |
is a | snp |
is | mentioned by |
dbSNP | rs1042194 |
dbSNP (classic) | rs1042194 |
ClinGen | rs1042194 |
ebi | rs1042194 |
HLI | rs1042194 |
Exac | rs1042194 |
Gnomad | rs1042194 |
Varsome | rs1042194 |
LitVar | rs1042194 |
Map | rs1042194 |
PheGenI | rs1042194 |
Biobank | rs1042194 |
1000 genomes | rs1042194 |
hgdp | rs1042194 |
ensembl | rs1042194 |
geneview | rs1042194 |
scholar | rs1042194 |
rs1042194 | |
pharmgkb | rs1042194 |
gwascentral | rs1042194 |
openSNP | rs1042194 |
23andMe | rs1042194 |
SNPshot | rs1042194 |
SNPdbe | rs1042194 |
MSV3d | rs1042194 |
GWAS Ctlg | rs1042194 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 28280103] Association of genetic variant and platelet function in patients undergoing neuroendovascular stenting.