rs16826658
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16826658(G;G) |
| Make rs16826658(G;T) |
| Make rs16826658(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 22159378 |
| Gene | LOC105376850 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16826658 |
| dbSNP (classic) | rs16826658 |
| ClinGen | rs16826658 |
| ebi | rs16826658 |
| HLI | rs16826658 |
| Exac | rs16826658 |
| Gnomad | rs16826658 |
| Varsome | rs16826658 |
| LitVar | rs16826658 |
| Map | rs16826658 |
| PheGenI | rs16826658 |
| Biobank | rs16826658 |
| 1000 genomes | rs16826658 |
| hgdp | rs16826658 |
| ensembl | rs16826658 |
| geneview | rs16826658 |
| scholar | rs16826658 |
| rs16826658 | |
| pharmgkb | rs16826658 |
| gwascentral | rs16826658 |
| openSNP | rs16826658 |
| 23andMe | rs16826658 |
| SNPshot | rs16826658 |
| SNPdbe | rs16826658 |
| MSV3d | rs16826658 |
| GWAS Ctlg | rs16826658 |
| GMAF | 0.3393 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20601957] A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese
[PMID 25682310] Analysis of WNT4 polymorphism in Chinese Han women with endometriosis
