rs726640
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs726640(C;T) |
| Make rs726640(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 159685728 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs726640 |
| dbSNP (classic) | rs726640 |
| ClinGen | rs726640 |
| ebi | rs726640 |
| HLI | rs726640 |
| Exac | rs726640 |
| Gnomad | rs726640 |
| Varsome | rs726640 |
| LitVar | rs726640 |
| Map | rs726640 |
| PheGenI | rs726640 |
| Biobank | rs726640 |
| 1000 genomes | rs726640 |
| hgdp | rs726640 |
| ensembl | rs726640 |
| geneview | rs726640 |
| scholar | rs726640 |
| rs726640 | |
| pharmgkb | rs726640 |
| gwascentral | rs726640 |
| openSNP | rs726640 |
| 23andMe | rs726640 |
| SNPshot | rs726640 |
| SNPdbe | rs726640 |
| MSV3d | rs726640 |
| GWAS Ctlg | rs726640 |
| GMAF | 0.03719 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| OMIM | 612780 |
| Desc | SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND |
| Variant | |
| Related | also |
| GWAS snp | |
|---|---|
| PMID | [PMID 22492993 ]
|
| Trait | |
| Title | C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans. |
| Risk Allele | |
| P-val | 2E-13 |
| Odds Ratio | 0.4400 None |
