rs10521339
From SNPedia
| some predictive power for baldness |
| Orientation | plus |
| Stabilized | plus |
| Make rs10521339(A;A) |
| Make rs10521339(A;T) |
| Make rs10521339(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 67288544 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10521339 |
| dbSNP (classic) | rs10521339 |
| ClinGen | rs10521339 |
| ebi | rs10521339 |
| HLI | rs10521339 |
| Exac | rs10521339 |
| Gnomad | rs10521339 |
| Varsome | rs10521339 |
| LitVar | rs10521339 |
| Map | rs10521339 |
| PheGenI | rs10521339 |
| Biobank | rs10521339 |
| 1000 genomes | rs10521339 |
| hgdp | rs10521339 |
| ensembl | rs10521339 |
| geneview | rs10521339 |
| scholar | rs10521339 |
| rs10521339 | |
| pharmgkb | rs10521339 |
| gwascentral | rs10521339 |
| openSNP | rs10521339 |
| 23andMe | rs10521339 |
| SNPshot | rs10521339 |
| SNPdbe | rs10521339 |
| MSV3d | rs10521339 |
| GWAS Ctlg | rs10521339 |
| GMAF | 0.3041 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
- lowest P value of 2.1×10-12 for rs10521339
- family based rs938059 shows the lowest P value (4.03×10-6) (table 3)
- rs6152 (P=6.66×10-10)
[PMID 17903294
] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
