rs2125443
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2125443(C;C) |
| Make rs2125443(C;T) |
| Make rs2125443(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 146849865 |
| Gene | PPP2R2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2125443 |
| dbSNP (classic) | rs2125443 |
| ClinGen | rs2125443 |
| ebi | rs2125443 |
| HLI | rs2125443 |
| Exac | rs2125443 |
| Gnomad | rs2125443 |
| Varsome | rs2125443 |
| LitVar | rs2125443 |
| Map | rs2125443 |
| PheGenI | rs2125443 |
| Biobank | rs2125443 |
| 1000 genomes | rs2125443 |
| hgdp | rs2125443 |
| ensembl | rs2125443 |
| geneview | rs2125443 |
| scholar | rs2125443 |
| rs2125443 | |
| pharmgkb | rs2125443 |
| gwascentral | rs2125443 |
| openSNP | rs2125443 |
| 23andMe | rs2125443 |
| SNPshot | rs2125443 |
| SNPdbe | rs2125443 |
| MSV3d | rs2125443 |
| GWAS Ctlg | rs2125443 |
| GMAF | 0.2259 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22369142
] Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- 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 NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d
