Difference between revisions of "Rs508485"
From SNPedia
OrientalBot (talk | contribs) (Set StabilizedOrientation) |
OrientalBot (talk | contribs) (Set on chip ancestryv2) |
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| Line 12: | Line 12: | ||
|geno2=(C;T) | |geno2=(C;T) | ||
|geno3=(T;T) | |geno3=(T;T) | ||
| − | |Gene_s=PIWIL4 | + | |Gene_s=LOC105369438,PIWIL4 |
|StabilizedOrientation=plus | |StabilizedOrientation=plus | ||
}}{{ population diversity | }}{{ population diversity | ||
| Line 39: | Line 39: | ||
{{on chip | 23andMe v4}} | {{on chip | 23andMe v4}} | ||
{{on chip | Affy GenomeWide 6}} | {{on chip | Affy GenomeWide 6}} | ||
| + | {{on chip | Ancestry v2}} | ||
{{on chip | FTDNA2}} | {{on chip | FTDNA2}} | ||
{{on chip | FTDNA}} | {{on chip | FTDNA}} | ||
| Line 44: | Line 45: | ||
{{on chip | Illumina Human 1M}} | {{on chip | Illumina Human 1M}} | ||
{{on chip | NatGeo2}} | {{on chip | NatGeo2}} | ||
| + | {{on chip | 23andMe v5}} | ||
| + | {{on chip | Ancestry v2c}} | ||
| + | {{on chip | Ancestry v2d}} | ||
Latest revision as of 03:42, 7 December 2019
| Orientation | plus |
| Stabilized | plus |
| Make rs508485(C;C) |
| Make rs508485(C;T) |
| Make rs508485(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 94621313 |
| Gene | LOC105369438, 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
