rs16979877
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16979877(A;A) |
| Make rs16979877(A;G) |
| Make rs16979877(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 56392982 |
| Gene | AURKA, CSTF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16979877 |
| dbSNP (classic) | rs16979877 |
| ClinGen | rs16979877 |
| ebi | rs16979877 |
| HLI | rs16979877 |
| Exac | rs16979877 |
| Gnomad | rs16979877 |
| Varsome | rs16979877 |
| LitVar | rs16979877 |
| Map | rs16979877 |
| PheGenI | rs16979877 |
| Biobank | rs16979877 |
| 1000 genomes | rs16979877 |
| hgdp | rs16979877 |
| ensembl | rs16979877 |
| geneview | rs16979877 |
| scholar | rs16979877 |
| rs16979877 | |
| pharmgkb | rs16979877 |
| gwascentral | rs16979877 |
| openSNP | rs16979877 |
| 23andMe | rs16979877 |
| SNPshot | rs16979877 |
| SNPdbe | rs16979877 |
| MSV3d | rs16979877 |
| GWAS Ctlg | rs16979877 |
| GMAF | 0.04775 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21630024] Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
