rs3810682
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common |
| Make rs3810682(C;C) |
| Make rs3810682(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 50910775 |
| Gene | BMP15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3810682 |
| dbSNP (classic) | rs3810682 |
| ClinGen | rs3810682 |
| ebi | rs3810682 |
| HLI | rs3810682 |
| Exac | rs3810682 |
| Gnomad | rs3810682 |
| Varsome | rs3810682 |
| LitVar | rs3810682 |
| Map | rs3810682 |
| PheGenI | rs3810682 |
| Biobank | rs3810682 |
| 1000 genomes | rs3810682 |
| hgdp | rs3810682 |
| ensembl | rs3810682 |
| geneview | rs3810682 |
| scholar | rs3810682 |
| rs3810682 | |
| pharmgkb | rs3810682 |
| gwascentral | rs3810682 |
| openSNP | rs3810682 |
| 23andMe | rs3810682 |
| SNPshot | rs3810682 |
| SNPdbe | rs3810682 |
| MSV3d | rs3810682 |
| GWAS Ctlg | rs3810682 |
| GMAF | 0.1475 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
Associated with ovarian failure
[PMID 17464588] Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure.
[PMID 18603647
] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
[PMID 18614612] Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.
| ClinVar | |
|---|---|
| Risk | rs3810682(C;C) |
| Alt | rs3810682(C;C) |
| Reference | Rs3810682(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified Ovarian Dysgenesis |
| Variation | info |
| Gene | BMP15 |
| CLNDBN | not specified Ovarian Dysgenesis |
| Reversed | 1 |
| HGVS | NC_000023.10:g.50653775C>G |
| CLNSRC | ClinVar GeneDx |
| CLNACC | RCV000123855.2, RCV000271182.1, |
