rs1048886
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1048886(A;A) |
| Make rs1048886(A;G) |
| Make rs1048886(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 70579486 |
| Gene | SDHAF4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048886 |
| dbSNP (classic) | rs1048886 |
| ClinGen | rs1048886 |
| ebi | rs1048886 |
| HLI | rs1048886 |
| Exac | rs1048886 |
| Gnomad | rs1048886 |
| Varsome | rs1048886 |
| LitVar | rs1048886 |
| Map | rs1048886 |
| PheGenI | rs1048886 |
| Biobank | rs1048886 |
| 1000 genomes | rs1048886 |
| hgdp | rs1048886 |
| ensembl | rs1048886 |
| geneview | rs1048886 |
| scholar | rs1048886 |
| rs1048886 | |
| pharmgkb | rs1048886 |
| gwascentral | rs1048886 |
| openSNP | rs1048886 |
| 23andMe | rs1048886 |
| SNPshot | rs1048886 |
| SNPdbe | rs1048886 |
| MSV3d | rs1048886 |
| GWAS Ctlg | rs1048886 |
| GMAF | 0.2048 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21490949 ]
|
| Trait | |
| Title | Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. |
| Risk Allele | G |
| P-val | 3E-8 |
| Odds Ratio | 1.5400 [1.32-1.80] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- 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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
