rs10774625
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10774625(A;A) |
| Make rs10774625(A;G) |
| Make rs10774625(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 111472415 |
| Gene | ATXN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10774625 |
| dbSNP (classic) | rs10774625 |
| ClinGen | rs10774625 |
| ebi | rs10774625 |
| HLI | rs10774625 |
| Exac | rs10774625 |
| Gnomad | rs10774625 |
| Varsome | rs10774625 |
| LitVar | rs10774625 |
| Map | rs10774625 |
| PheGenI | rs10774625 |
| Biobank | rs10774625 |
| 1000 genomes | rs10774625 |
| hgdp | rs10774625 |
| ensembl | rs10774625 |
| geneview | rs10774625 |
| scholar | rs10774625 |
| rs10774625 | |
| pharmgkb | rs10774625 |
| gwascentral | rs10774625 |
| openSNP | rs10774625 |
| 23andMe | rs10774625 |
| SNPshot | rs10774625 |
| SNPdbe | rs10774625 |
| MSV3d | rs10774625 |
| GWAS Ctlg | rs10774625 |
| GMAF | 0.225 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21060863 ]
|
| Trait | |
| Title | Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo |
| Risk Allele | A |
| P-val | 2E-13 |
| Odds Ratio | 1.5000 [1.11-1.89] um increase |
[PMID 23844121] Thrombotic Antiphospholipid Syndrome Shows Strong Haplotypic Association with SH2B3-ATXN2 Locus
