rs990324
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs990324(A;A) |
| Make rs990324(A;G) |
| Make rs990324(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 32813108 |
| Gene | LINC00423 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs990324 |
| dbSNP (classic) | rs990324 |
| ClinGen | rs990324 |
| ebi | rs990324 |
| HLI | rs990324 |
| Exac | rs990324 |
| Gnomad | rs990324 |
| Varsome | rs990324 |
| LitVar | rs990324 |
| Map | rs990324 |
| PheGenI | rs990324 |
| Biobank | rs990324 |
| 1000 genomes | rs990324 |
| hgdp | rs990324 |
| ensembl | rs990324 |
| geneview | rs990324 |
| scholar | rs990324 |
| rs990324 | |
| pharmgkb | rs990324 |
| gwascentral | rs990324 |
| openSNP | rs990324 |
| 23andMe | rs990324 |
| SNPshot | rs990324 |
| SNPdbe | rs990324 |
| MSV3d | rs990324 |
| GWAS Ctlg | rs990324 |
| GMAF | 0.1699 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21116278 ]
|
| Trait | |
| Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 0.0064 [NR] unit decrease (interaction) |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- 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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
