rs1172822
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1172822(C;C) |
| Make rs1172822(C;T) |
| Make rs1172822(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 55308477 |
| Gene | BRSK1, TMEM150B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1172822 |
| dbSNP (classic) | rs1172822 |
| ClinGen | rs1172822 |
| ebi | rs1172822 |
| HLI | rs1172822 |
| Exac | rs1172822 |
| Gnomad | rs1172822 |
| Varsome | rs1172822 |
| LitVar | rs1172822 |
| Map | rs1172822 |
| PheGenI | rs1172822 |
| Biobank | rs1172822 |
| 1000 genomes | rs1172822 |
| hgdp | rs1172822 |
| ensembl | rs1172822 |
| geneview | rs1172822 |
| scholar | rs1172822 |
| rs1172822 | |
| pharmgkb | rs1172822 |
| gwascentral | rs1172822 |
| openSNP | rs1172822 |
| 23andMe | rs1172822 |
| SNPshot | rs1172822 |
| SNPdbe | rs1172822 |
| MSV3d | rs1172822 |
| GWAS Ctlg | rs1172822 |
| GMAF | 0.2691 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog rs1172822(T) Menopause about 25 weeks earlier
| GWAS snp | |
|---|---|
| PMID | [PMID 19448619 |
| Trait | Menopause |
| Title | Loci at chromosomes 13, 19 and 20 influence age at natural menopause. |
| Risk Allele | T |
| P-val | 6E-11 |
| Odds Ratio | 0.39 [0.27-0.51] years younger |
| GWAS snp | |
|---|---|
| PMID | [PMID 19448621 |
| Trait | Menarche and menopause (age at onset) |
| Title | Genome-wide association studies identify loci associated with age at menarche and age at natural menopause |
| Risk Allele | T |
| P-val | 2E-19 |
| Odds Ratio | 0.49 [0.38-0.60] years younger |
[PMID 19664201
] Genetic and genomic insights into age at natural menopause.
[PMID 23508249
] Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study
[PMID 23536822
] Evaluating GWAS-Identified SNPs for Age at Natural Menopause among Chinese Women
[PMID 23592221] Shared genetic factors for age at natural menopause in Iranian and European women
[PMID 23360674] Genetic variation may modify ovarian reserve in female childhood cancer survivors.
