rs7748513
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common genotype |
| Make rs7748513(A;G) |
| Make rs7748513(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 41160234 |
| Gene | LOC105375056, TREM2, TREML1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7748513 |
| dbSNP (classic) | rs7748513 |
| ClinGen | rs7748513 |
| ebi | rs7748513 |
| HLI | rs7748513 |
| Exac | rs7748513 |
| Gnomad | rs7748513 |
| Varsome | rs7748513 |
| LitVar | rs7748513 |
| Map | rs7748513 |
| PheGenI | rs7748513 |
| Biobank | rs7748513 |
| 1000 genomes | rs7748513 |
| hgdp | rs7748513 |
| ensembl | rs7748513 |
| geneview | rs7748513 |
| scholar | rs7748513 |
| rs7748513 | |
| pharmgkb | rs7748513 |
| gwascentral | rs7748513 |
| openSNP | rs7748513 |
| 23andMe | rs7748513 |
| SNPshot | rs7748513 |
| SNPdbe | rs7748513 |
| MSV3d | rs7748513 |
| GWAS Ctlg | rs7748513 |
| GMAF | 0.1354 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22939635 ]
|
| Trait | C-reactive protein |
| Title | Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women. |
| Risk Allele | G |
| P-val | 1E-10 |
| Odds Ratio | NR NR |
[PMID 19019460] No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.
