rs17170899
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs17170899(C;T) |
| Make rs17170899(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 137040361 |
| Gene | SPOCK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17170899 |
| dbSNP (classic) | rs17170899 |
| ClinGen | rs17170899 |
| ebi | rs17170899 |
| HLI | rs17170899 |
| Exac | rs17170899 |
| Gnomad | rs17170899 |
| Varsome | rs17170899 |
| LitVar | rs17170899 |
| Map | rs17170899 |
| PheGenI | rs17170899 |
| Biobank | rs17170899 |
| 1000 genomes | rs17170899 |
| hgdp | rs17170899 |
| ensembl | rs17170899 |
| geneview | rs17170899 |
| scholar | rs17170899 |
| rs17170899 | |
| pharmgkb | rs17170899 |
| gwascentral | rs17170899 |
| openSNP | rs17170899 |
| 23andMe | rs17170899 |
| SNPshot | rs17170899 |
| SNPdbe | rs17170899 |
| MSV3d | rs17170899 |
| GWAS Ctlg | rs17170899 |
| GMAF | 0.04454 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22369142
] Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5
