rs1321311
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1321311(G;G) |
| Make rs1321311(G;T) |
| Make rs1321311(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 36655123 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1321311 |
| dbSNP (classic) | rs1321311 |
| ClinGen | rs1321311 |
| ebi | rs1321311 |
| HLI | rs1321311 |
| Exac | rs1321311 |
| Gnomad | rs1321311 |
| Varsome | rs1321311 |
| LitVar | rs1321311 |
| Map | rs1321311 |
| PheGenI | rs1321311 |
| Biobank | rs1321311 |
| 1000 genomes | rs1321311 |
| hgdp | rs1321311 |
| ensembl | rs1321311 |
| geneview | rs1321311 |
| scholar | rs1321311 |
| rs1321311 | |
| pharmgkb | rs1321311 |
| gwascentral | rs1321311 |
| openSNP | rs1321311 |
| 23andMe | rs1321311 |
| SNPshot | rs1321311 |
| SNPdbe | rs1321311 |
| MSV3d | rs1321311 |
| GWAS Ctlg | rs1321311 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062063] |
| Trait | Electrocardiographic traits |
| Title | Several common variants modulate heart rate, PR interval and QRS duration |
| Risk Allele | T |
| P-val | 3E-10 |
| Odds Ratio | 6.52 [4.50-8.55] % SD increase |
[PMID 22634755
] Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
[PMID 26078566] Association of colorectal cancer susceptibility variants with esophageal cancer in a Chinese population
[PMID 29147930] SNP association study in PMS2-associated Lynch syndrome.
