rs17003221
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs17003221(C;T) |
| Make rs17003221(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 50916280 |
| Gene | BMP15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17003221 |
| dbSNP (classic) | rs17003221 |
| ClinGen | rs17003221 |
| ebi | rs17003221 |
| HLI | rs17003221 |
| Exac | rs17003221 |
| Gnomad | rs17003221 |
| Varsome | rs17003221 |
| LitVar | rs17003221 |
| Map | rs17003221 |
| PheGenI | rs17003221 |
| Biobank | rs17003221 |
| 1000 genomes | rs17003221 |
| hgdp | rs17003221 |
| ensembl | rs17003221 |
| geneview | rs17003221 |
| scholar | rs17003221 |
| rs17003221 | |
| pharmgkb | rs17003221 |
| gwascentral | rs17003221 |
| openSNP | rs17003221 |
| 23andMe | rs17003221 |
| SNPshot | rs17003221 |
| SNPdbe | rs17003221 |
| MSV3d | rs17003221 |
| GWAS Ctlg | rs17003221 |
| GMAF | 0.1378 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18614612
] Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.
| ClinVar | |
|---|---|
| Risk | rs17003221(T;T) |
| Alt | rs17003221(T;T) |
| Reference | Rs17003221(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified Ovarian Dysgenesis |
| Variation | info |
| Gene | BMP15 |
| CLNDBN | not specified Ovarian Dysgenesis |
| Reversed | 0 |
| HGVS | NC_000023.10:g.50659280C>T |
| CLNSRC | |
| CLNACC | RCV000245391.2, RCV000292718.1, |
