rs2834442
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2834442(A;A) |
| Make rs2834442(A;T) |
| Make rs2834442(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 34318486 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2834442 |
| dbSNP (classic) | rs2834442 |
| ClinGen | rs2834442 |
| ebi | rs2834442 |
| HLI | rs2834442 |
| Exac | rs2834442 |
| Gnomad | rs2834442 |
| Varsome | rs2834442 |
| LitVar | rs2834442 |
| Map | rs2834442 |
| PheGenI | rs2834442 |
| Biobank | rs2834442 |
| 1000 genomes | rs2834442 |
| hgdp | rs2834442 |
| ensembl | rs2834442 |
| geneview | rs2834442 |
| scholar | rs2834442 |
| rs2834442 | |
| pharmgkb | rs2834442 |
| gwascentral | rs2834442 |
| openSNP | rs2834442 |
| 23andMe | rs2834442 |
| SNPshot | rs2834442 |
| SNPdbe | rs2834442 |
| MSV3d | rs2834442 |
| GWAS Ctlg | rs2834442 |
| GMAF | 0.3838 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 5E-12 |
| Odds Ratio | 0.0300 [NR] meters increase |
[PMID 18676988] A high-density association screen of 155 ion transport genes for involvement with common migraine.
