rs1819698
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common/normal |
| Make rs1819698(A;A) |
| Make rs1819698(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 119422896 |
| Gene | HSD3B2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1819698 |
| dbSNP (classic) | rs1819698 |
| ClinGen | rs1819698 |
| ebi | rs1819698 |
| HLI | rs1819698 |
| Exac | rs1819698 |
| Gnomad | rs1819698 |
| Varsome | rs1819698 |
| LitVar | rs1819698 |
| Map | rs1819698 |
| PheGenI | rs1819698 |
| Biobank | rs1819698 |
| 1000 genomes | rs1819698 |
| hgdp | rs1819698 |
| ensembl | rs1819698 |
| geneview | rs1819698 |
| scholar | rs1819698 |
| rs1819698 | |
| pharmgkb | rs1819698 |
| gwascentral | rs1819698 |
| openSNP | rs1819698 |
| 23andMe | rs1819698 |
| SNPshot | rs1819698 |
| SNPdbe | rs1819698 |
| MSV3d | rs1819698 |
| GWAS Ctlg | rs1819698 |
| GMAF | 0.2691 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22638611] Estrogen synthesis genes CYP19A1, HSD3B1, and HSD3B2 in hypertensive disorders of pregnancy
[PMID 19168589
] Variants in hormone-related genes and the risk of biliary tract cancers and stones: a population-based study in China.
[PMID 20660004] Association of HSD3B1 and HSD3B2 gene polymorphisms with essential hypertension, aldosterone level, and left ventricular structure.
| ClinVar | |
|---|---|
| Risk | rs1819698(A;A) |
| Alt | rs1819698(A;A) |
| Reference | Rs1819698(G;G) |
| Significance | Non-pathogenic |
| Disease | Congenital adrenal hyperplasia |
| Variation | info |
| Gene | HSD3B2 |
| CLNDBN | Congenital adrenal hyperplasia |
| Reversed | 1 |
| HGVS | NC_000001.10:g.119965519C>T |
| CLNSRC | |
| CLNACC | RCV000335090.1, |
