Difference between revisions of "Rs508485"
From SNPedia
SNPediaBot (talk | contribs) m (Set on chip) |
SNPediaBot (talk | contribs) m (set GMAF to 0.4734) |
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|position=94354479 | |position=94354479 | ||
|Orientation=plus | |Orientation=plus | ||
| − | |GMAF=0. | + | |GMAF=0.4734 |
| + | |Assembly=GRCh37 | ||
| + | |GenomeBuild=37.1 | ||
| + | |dbSNPBuild=132 | ||
|geno1=(C;C) | |geno1=(C;C) | ||
|geno2=(C;T) | |geno2=(C;T) | ||
|geno3=(T;T) | |geno3=(T;T) | ||
| − | |||
| − | |||
| − | |||
}} | }} | ||
{{ population diversity | {{ population diversity | ||
Revision as of 00:32, 1 April 2014
| Orientation | plus |
| Make rs508485(C;C) |
| Make rs508485(C;T) |
| Make rs508485(T;T) |
| Reference | GRCh37 37.1/132 |
| Chromosome | 11 |
| Position | 94354479 |
| Gene | PIWIL4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs508485 |
| dbSNP (classic) | rs508485 |
| ClinGen | rs508485 |
| ebi | rs508485 |
| HLI | rs508485 |
| Exac | rs508485 |
| Gnomad | rs508485 |
| Varsome | rs508485 |
| LitVar | rs508485 |
| Map | rs508485 |
| PheGenI | rs508485 |
| Biobank | rs508485 |
| 1000 genomes | rs508485 |
| hgdp | rs508485 |
| ensembl | rs508485 |
| geneview | rs508485 |
| scholar | rs508485 |
| rs508485 | |
| pharmgkb | rs508485 |
| gwascentral | rs508485 |
| openSNP | rs508485 |
| 23andMe | rs508485 |
| SNPshot | rs508485 |
| SNPdbe | rs508485 |
| MSV3d | rs508485 |
| GWAS Ctlg | rs508485 |
| GMAF | 0.4734 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20940137] Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population
