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