rs2990510
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2990510(G;G) |
| Make rs2990510(G;T) |
| Make rs2990510(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 197051528 |
| Gene | F13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2990510 |
| dbSNP (classic) | rs2990510 |
| ClinGen | rs2990510 |
| ebi | rs2990510 |
| HLI | rs2990510 |
| Exac | rs2990510 |
| Gnomad | rs2990510 |
| Varsome | rs2990510 |
| LitVar | rs2990510 |
| Map | rs2990510 |
| PheGenI | rs2990510 |
| Biobank | rs2990510 |
| 1000 genomes | rs2990510 |
| hgdp | rs2990510 |
| ensembl | rs2990510 |
| geneview | rs2990510 |
| scholar | rs2990510 |
| rs2990510 | |
| pharmgkb | rs2990510 |
| gwascentral | rs2990510 |
| openSNP | rs2990510 |
| 23andMe | rs2990510 |
| SNPshot | rs2990510 |
| SNPdbe | rs2990510 |
| MSV3d | rs2990510 |
| GWAS Ctlg | rs2990510 |
| GMAF | 0.2397 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22704111 ]
|
| Trait | |
| Title | Pilot Genome-Wide Association Search Identifies Potential Loci for Risk of Erectile Dysfunction in Type 1 Diabetes Using the DCCT/EDIC Study Cohort. |
| Risk Allele | G |
| P-val | 0.000006 |
| Odds Ratio | None None |
[PMID 18541031] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.
