rs1810636
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1810636(G;G) |
| Make rs1810636(G;T) |
| Make rs1810636(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 2674279 |
| Gene | LOC105372507 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1810636 |
| dbSNP (classic) | rs1810636 |
| ClinGen | rs1810636 |
| ebi | rs1810636 |
| HLI | rs1810636 |
| Exac | rs1810636 |
| Gnomad | rs1810636 |
| Varsome | rs1810636 |
| LitVar | rs1810636 |
| Map | rs1810636 |
| PheGenI | rs1810636 |
| Biobank | rs1810636 |
| 1000 genomes | rs1810636 |
| hgdp | rs1810636 |
| ensembl | rs1810636 |
| geneview | rs1810636 |
| scholar | rs1810636 |
| rs1810636 | |
| pharmgkb | rs1810636 |
| gwascentral | rs1810636 |
| openSNP | rs1810636 |
| 23andMe | rs1810636 |
| SNPshot | rs1810636 |
| SNPdbe | rs1810636 |
| MSV3d | rs1810636 |
| GWAS Ctlg | rs1810636 |
| GMAF | 0.3802 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
Mentioned in retracted [PMID 20595579]
[PMID 22105264
] Identification of six Loci associated with pelvic organ prolapse using genome-wide association analysis
