rs7636
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs7636(C;C) |
| Make rs7636(C;T) |
| Make rs7636(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 100892456 |
| Gene | ACHE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7636 |
| dbSNP (classic) | rs7636 |
| ClinGen | rs7636 |
| ebi | rs7636 |
| HLI | rs7636 |
| Exac | rs7636 |
| Gnomad | rs7636 |
| Varsome | rs7636 |
| LitVar | rs7636 |
| Map | rs7636 |
| PheGenI | rs7636 |
| Biobank | rs7636 |
| 1000 genomes | rs7636 |
| hgdp | rs7636 |
| ensembl | rs7636 |
| geneview | rs7636 |
| scholar | rs7636 |
| rs7636 | |
| pharmgkb | rs7636 |
| gwascentral | rs7636 |
| openSNP | rs7636 |
| 23andMe | rs7636 |
| SNPshot | rs7636 |
| SNPdbe | rs7636 |
| MSV3d | rs7636 |
| GWAS Ctlg | rs7636 |
| GMAF | 0.1001 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21490949 ]
|
| Trait | |
| Title | Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. |
| Risk Allele | A |
| P-val | 0.000005 |
| Odds Ratio | 1.8500 [1.42-2.41] |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.
[PMID 16251468] Survey of allelic expression using EST mining.
