rs10845271
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10845271(C;C) |
| Make rs10845271(C;T) |
| Make rs10845271(T;T) |
| Reference | GRCh37.p2 37.2/134 |
| Chromosome | 12 |
| Position | 10991202 |
| Gene | PRH1, PRH1-PRR4, PRH1-TAS2R14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10845271 |
| dbSNP (classic) | rs10845271 |
| ClinGen | rs10845271 |
| ebi | rs10845271 |
| HLI | rs10845271 |
| Exac | rs10845271 |
| Gnomad | rs10845271 |
| Varsome | rs10845271 |
| LitVar | rs10845271 |
| Map | rs10845271 |
| PheGenI | rs10845271 |
| Biobank | rs10845271 |
| 1000 genomes | rs10845271 |
| hgdp | rs10845271 |
| ensembl | rs10845271 |
| geneview | rs10845271 |
| scholar | rs10845271 |
| rs10845271 | |
| pharmgkb | rs10845271 |
| gwascentral | rs10845271 |
| openSNP | rs10845271 |
| 23andMe | rs10845271 |
| SNPshot | rs10845271 |
| SNPdbe | rs10845271 |
| MSV3d | rs10845271 |
| GWAS Ctlg | rs10845271 |
| GMAF | 0.4114 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs10845271 | |
|---|---|
| PubMed | [PMID 16175505 ]
|
| Affy Probeset | SNP_A-2027345 |
| Affy Orientation | same |
| On GW 5.0 | 1 |
| Alleles A/B | C/T |
| Ancestral | C |
| Population | Caucasian |
| Allele | C |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | 1.23 |
| Odds Ratio Hom | 1.58 |
| Odds Ratio All | |
| Disease | Myocardial Infarction (MI) |
rs10845271 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocardial Infarction 1.23 times for heterozygotes (CT) and 1.58 times for homozygotes (CC) [PMID 16175505]
