rs1867631
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1867631(A;A) |
| Make rs1867631(A;C) |
| Make rs1867631(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 66580443 |
| Gene | SGIP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1867631 |
| dbSNP (classic) | rs1867631 |
| ClinGen | rs1867631 |
| ebi | rs1867631 |
| HLI | rs1867631 |
| Exac | rs1867631 |
| Gnomad | rs1867631 |
| Varsome | rs1867631 |
| LitVar | rs1867631 |
| Map | rs1867631 |
| PheGenI | rs1867631 |
| Biobank | rs1867631 |
| 1000 genomes | rs1867631 |
| hgdp | rs1867631 |
| ensembl | rs1867631 |
| geneview | rs1867631 |
| scholar | rs1867631 |
| rs1867631 | |
| pharmgkb | rs1867631 |
| gwascentral | rs1867631 |
| openSNP | rs1867631 |
| 23andMe | rs1867631 |
| SNPshot | rs1867631 |
| SNPdbe | rs1867631 |
| MSV3d | rs1867631 |
| GWAS Ctlg | rs1867631 |
| GMAF | 0.3893 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23307926 ]
|
| Trait | Menopause (age at onset) |
| Title | A genome-wide association study of early menopause and the combined impact of identified variants. |
| Risk Allele | A |
| P-val | 5E-6 |
| Odds Ratio | .11 [0.060-0.154] years decrease |
