rs1534166
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1534166(A;A) |
| Make rs1534166(A;G) |
| Make rs1534166(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 133818223 |
| Gene | SRPRB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1534166 |
| dbSNP (classic) | rs1534166 |
| ClinGen | rs1534166 |
| ebi | rs1534166 |
| HLI | rs1534166 |
| Exac | rs1534166 |
| Gnomad | rs1534166 |
| Varsome | rs1534166 |
| LitVar | rs1534166 |
| Map | rs1534166 |
| PheGenI | rs1534166 |
| Biobank | rs1534166 |
| 1000 genomes | rs1534166 |
| hgdp | rs1534166 |
| ensembl | rs1534166 |
| geneview | rs1534166 |
| scholar | rs1534166 |
| rs1534166 | |
| pharmgkb | rs1534166 |
| gwascentral | rs1534166 |
| openSNP | rs1534166 |
| 23andMe | rs1534166 |
| SNPshot | rs1534166 |
| SNPdbe | rs1534166 |
| MSV3d | rs1534166 |
| GWAS Ctlg | rs1534166 |
| GMAF | 0.2544 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21665994 |
| Trait | |
| Title | Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. |
| Risk Allele | A |
| P-val | 2E-17 |
| Odds Ratio | 0.2890 [0.22-0.36] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
