rs4906172
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4906172(A;A) |
| Make rs4906172(A;C) |
| Make rs4906172(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 101988596 |
| Gene | DYNC1H1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4906172 |
| dbSNP (classic) | rs4906172 |
| ClinGen | rs4906172 |
| ebi | rs4906172 |
| HLI | rs4906172 |
| Exac | rs4906172 |
| Gnomad | rs4906172 |
| Varsome | rs4906172 |
| LitVar | rs4906172 |
| Map | rs4906172 |
| PheGenI | rs4906172 |
| Biobank | rs4906172 |
| 1000 genomes | rs4906172 |
| hgdp | rs4906172 |
| ensembl | rs4906172 |
| geneview | rs4906172 |
| scholar | rs4906172 |
| rs4906172 | |
| pharmgkb | rs4906172 |
| gwascentral | rs4906172 |
| openSNP | rs4906172 |
| 23andMe | rs4906172 |
| SNPshot | rs4906172 |
| SNPdbe | rs4906172 |
| MSV3d | rs4906172 |
| GWAS Ctlg | rs4906172 |
| GMAF | 0.3517 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19448619 ]
|
| Trait | Menopause |
| Title | Loci at chromosomes 13, 19 and 20 influence age at natural menopause. |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | 0.36 [0.21-0.51] years younger |
