rs2076310
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2076310(C;C) |
| Make rs2076310(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 33198257 |
| Gene | RXRB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2076310 |
| dbSNP (classic) | rs2076310 |
| ClinGen | rs2076310 |
| ebi | rs2076310 |
| HLI | rs2076310 |
| Exac | rs2076310 |
| Gnomad | rs2076310 |
| Varsome | rs2076310 |
| LitVar | rs2076310 |
| Map | rs2076310 |
| PheGenI | rs2076310 |
| Biobank | rs2076310 |
| 1000 genomes | rs2076310 |
| hgdp | rs2076310 |
| ensembl | rs2076310 |
| geneview | rs2076310 |
| scholar | rs2076310 |
| rs2076310 | |
| pharmgkb | rs2076310 |
| gwascentral | rs2076310 |
| openSNP | rs2076310 |
| 23andMe | rs2076310 |
| SNPshot | rs2076310 |
| SNPdbe | rs2076310 |
| MSV3d | rs2076310 |
| GWAS Ctlg | rs2076310 |
| GMAF | 0.3636 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20587610] Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection
[PMID 18375961
] Polymorphism of genes related to insulin sensitivity and the risk of biliary tract cancer and biliary stone: a population-based case-control study in Shanghai, China.
