rs598126
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs598126(C;C) |
| Make rs598126(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 42564502 |
| Gene | COASY |
| is a | snp |
| is | mentioned by |
| dbSNP | rs598126 |
| dbSNP (classic) | rs598126 |
| ClinGen | rs598126 |
| ebi | rs598126 |
| HLI | rs598126 |
| Exac | rs598126 |
| Gnomad | rs598126 |
| Varsome | rs598126 |
| LitVar | rs598126 |
| Map | rs598126 |
| PheGenI | rs598126 |
| Biobank | rs598126 |
| 1000 genomes | rs598126 |
| hgdp | rs598126 |
| ensembl | rs598126 |
| geneview | rs598126 |
| scholar | rs598126 |
| rs598126 | |
| pharmgkb | rs598126 |
| gwascentral | rs598126 |
| openSNP | rs598126 |
| 23andMe | rs598126 |
| SNPshot | rs598126 |
| SNPdbe | rs598126 |
| MSV3d | rs598126 |
| GWAS Ctlg | rs598126 |
| GMAF | 0.4725 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21092186
] Polymorphisms in genes involved in the estrogen pathway and mammographic density
[PMID 18843021] HSD17B1 genetic variants and hormone receptor-defined breast cancer.
[PMID 19015200] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.
| ClinVar | |
|---|---|
| Risk | rs598126(C;C) |
| Alt | rs598126(C;C) |
| Reference | Rs598126(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | COASY |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000017.10:g.40716520A>G |
| CLNSRC | |
| CLNACC | RCV000436954.1, |
