rs9901756
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9901756(A;A) |
| Make rs9901756(A;C) |
| Make rs9901756(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 34137135 |
| Gene | ASIC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9901756 |
| dbSNP (classic) | rs9901756 |
| ClinGen | rs9901756 |
| ebi | rs9901756 |
| HLI | rs9901756 |
| Exac | rs9901756 |
| Gnomad | rs9901756 |
| Varsome | rs9901756 |
| LitVar | rs9901756 |
| Map | rs9901756 |
| PheGenI | rs9901756 |
| Biobank | rs9901756 |
| 1000 genomes | rs9901756 |
| hgdp | rs9901756 |
| ensembl | rs9901756 |
| geneview | rs9901756 |
| scholar | rs9901756 |
| rs9901756 | |
| pharmgkb | rs9901756 |
| gwascentral | rs9901756 |
| openSNP | rs9901756 |
| 23andMe | rs9901756 |
| SNPshot | rs9901756 |
| SNPdbe | rs9901756 |
| MSV3d | rs9901756 |
| GWAS Ctlg | rs9901756 |
| GMAF | 0.1042 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22493691 ]
|
| Trait | |
| Title | Novel associations for hypothyroidism include known autoimmune risk loci. |
| Risk Allele | A |
| P-val | 0.000007 |
| Odds Ratio | 1.2100 None |
