rs2002555
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2002555(C;C) |
| Make rs2002555(C;T) |
| Make rs2002555(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 53423453 |
| Gene | AMHR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2002555 |
| dbSNP (classic) | rs2002555 |
| ClinGen | rs2002555 |
| ebi | rs2002555 |
| HLI | rs2002555 |
| Exac | rs2002555 |
| Gnomad | rs2002555 |
| Varsome | rs2002555 |
| LitVar | rs2002555 |
| Map | rs2002555 |
| PheGenI | rs2002555 |
| Biobank | rs2002555 |
| 1000 genomes | rs2002555 |
| hgdp | rs2002555 |
| ensembl | rs2002555 |
| geneview | rs2002555 |
| scholar | rs2002555 |
| rs2002555 | |
| pharmgkb | rs2002555 |
| gwascentral | rs2002555 |
| openSNP | rs2002555 |
| 23andMe | rs2002555 |
| SNPshot | rs2002555 |
| SNPdbe | rs2002555 |
| MSV3d | rs2002555 |
| GWAS Ctlg | rs2002555 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25379134
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[PMID 31115963] The implication of single-nucleotide polymorphisms in ovarian hyperstimulation syndrome.
