rs2282032
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2282032(G;G) |
| Make rs2282032(G;T) |
| Make rs2282032(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 90292547 |
| Gene | NRDE2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2282032 |
| dbSNP (classic) | rs2282032 |
| ClinGen | rs2282032 |
| ebi | rs2282032 |
| HLI | rs2282032 |
| Exac | rs2282032 |
| Gnomad | rs2282032 |
| Varsome | rs2282032 |
| LitVar | rs2282032 |
| Map | rs2282032 |
| PheGenI | rs2282032 |
| Biobank | rs2282032 |
| 1000 genomes | rs2282032 |
| hgdp | rs2282032 |
| ensembl | rs2282032 |
| geneview | rs2282032 |
| scholar | rs2282032 |
| rs2282032 | |
| pharmgkb | rs2282032 |
| gwascentral | rs2282032 |
| openSNP | rs2282032 |
| 23andMe | rs2282032 |
| SNPshot | rs2282032 |
| SNPdbe | rs2282032 |
| MSV3d | rs2282032 |
| GWAS Ctlg | rs2282032 |
| GMAF | 0.1387 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20834067 |
| Trait | |
| Title | Joint influence of small-effect genetic variants on human longevity. |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | None None |
[PMID 11022011
] A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 14
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
