rs603446
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs603446(C;C) |
| Make rs603446(C;T) |
| Make rs603446(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 116783719 |
| Gene | ZPR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs603446 |
| dbSNP (classic) | rs603446 |
| ClinGen | rs603446 |
| ebi | rs603446 |
| HLI | rs603446 |
| Exac | rs603446 |
| Gnomad | rs603446 |
| Varsome | rs603446 |
| LitVar | rs603446 |
| Map | rs603446 |
| PheGenI | rs603446 |
| Biobank | rs603446 |
| 1000 genomes | rs603446 |
| hgdp | rs603446 |
| ensembl | rs603446 |
| geneview | rs603446 |
| scholar | rs603446 |
| rs603446 | |
| pharmgkb | rs603446 |
| gwascentral | rs603446 |
| openSNP | rs603446 |
| 23andMe | rs603446 |
| SNPshot | rs603446 |
| SNPdbe | rs603446 |
| MSV3d | rs603446 |
| GWAS Ctlg | rs603446 |
| GMAF | 0.3131 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21909109] |
| Trait | |
| Title | Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. |
| Risk Allele | T |
| P-val | 2E-86 |
| Odds Ratio | 0.0876 [0.079-0.096] mg/dL decrease |
[PMID 19047183
] GRM7 variants confer susceptibility to age-related hearing impairment.
[PMID 20017964] Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic.
[PMID 20018031] The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study.
