rs10248351
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs10248351(C;C) |
| Make rs10248351(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 88852128 |
| Gene | ZNF804B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10248351 |
| dbSNP (classic) | rs10248351 |
| ClinGen | rs10248351 |
| ebi | rs10248351 |
| HLI | rs10248351 |
| Exac | rs10248351 |
| Gnomad | rs10248351 |
| Varsome | rs10248351 |
| LitVar | rs10248351 |
| Map | rs10248351 |
| PheGenI | rs10248351 |
| Biobank | rs10248351 |
| 1000 genomes | rs10248351 |
| hgdp | rs10248351 |
| ensembl | rs10248351 |
| geneview | rs10248351 |
| scholar | rs10248351 |
| rs10248351 | |
| pharmgkb | rs10248351 |
| gwascentral | rs10248351 |
| openSNP | rs10248351 |
| 23andMe | rs10248351 |
| SNPshot | rs10248351 |
| SNPdbe | rs10248351 |
| MSV3d | rs10248351 |
| GWAS Ctlg | rs10248351 |
| GMAF | 0.04867 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22493691 ]
|
| Trait | |
| Title | Novel associations for hypothyroidism include known autoimmune risk loci. |
| Risk Allele | C |
| P-val | 0.000007 |
| Odds Ratio | 1.8430 None |
