rs10276619
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10276619(A;A) |
| Make rs10276619(A;G) |
| Make rs10276619(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 50273756 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10276619 |
| dbSNP (classic) | rs10276619 |
| ClinGen | rs10276619 |
| ebi | rs10276619 |
| HLI | rs10276619 |
| Exac | rs10276619 |
| Gnomad | rs10276619 |
| Varsome | rs10276619 |
| LitVar | rs10276619 |
| Map | rs10276619 |
| PheGenI | rs10276619 |
| Biobank | rs10276619 |
| 1000 genomes | rs10276619 |
| hgdp | rs10276619 |
| ensembl | rs10276619 |
| geneview | rs10276619 |
| scholar | rs10276619 |
| rs10276619 | |
| pharmgkb | rs10276619 |
| gwascentral | rs10276619 |
| openSNP | rs10276619 |
| 23andMe | rs10276619 |
| SNPshot | rs10276619 |
| SNPdbe | rs10276619 |
| MSV3d | rs10276619 |
| GWAS Ctlg | rs10276619 |
| GMAF | 0.4541 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19668339 |
| Trait | Hippocampal atrophy |
| Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | NR NR |
| GWAS snp | |
|---|---|
| PMID | [PMID 23273568 |
| Trait | Systemic lupus erythematosus |
| Title | Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. |
| Risk Allele | G |
| P-val | 6E-6 |
| Odds Ratio | 1.18 |
