rs5748469
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs5748469(A;A) |
| Make rs5748469(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19919576 |
| Gene | TXNRD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5748469 |
| dbSNP (classic) | rs5748469 |
| ClinGen | rs5748469 |
| ebi | rs5748469 |
| HLI | rs5748469 |
| Exac | rs5748469 |
| Gnomad | rs5748469 |
| Varsome | rs5748469 |
| LitVar | rs5748469 |
| Map | rs5748469 |
| PheGenI | rs5748469 |
| Biobank | rs5748469 |
| 1000 genomes | rs5748469 |
| hgdp | rs5748469 |
| ensembl | rs5748469 |
| geneview | rs5748469 |
| scholar | rs5748469 |
| rs5748469 | |
| pharmgkb | rs5748469 |
| gwascentral | rs5748469 |
| openSNP | rs5748469 |
| 23andMe | rs5748469 |
| SNPshot | rs5748469 |
| SNPdbe | rs5748469 |
| MSV3d | rs5748469 |
| GWAS Ctlg | rs5748469 |
| GMAF | 0.4894 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20178852] Association Study between Polymorphisms in Selenoprotein Genes and Susceptibility to Kashin-Beck Disease
[PMID 17601350
] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.
[PMID 24058403] Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan population
| ClinVar | |
|---|---|
| Risk | rs5748469(A;A) |
| Alt | rs5748469(A;A) |
| Reference | Rs5748469(C;C) |
| Significance | Non-pathogenic |
| Disease | Cardiovascular phenotype not specified |
| Variation | info |
| Gene | TXNRD2 |
| CLNDBN | Cardiovascular phenotype not specified |
| Reversed | 0 |
| HGVS | NC_000022.10:g.19907099C>A |
| CLNSRC | |
| CLNACC | RCV000250227.1, RCV000445075.1, |
