rs10488764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10488764(A;A) |
| Make rs10488764(A;G) |
| Make rs10488764(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 110460907 |
| Gene | FDX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10488764 |
| dbSNP (classic) | rs10488764 |
| ClinGen | rs10488764 |
| ebi | rs10488764 |
| HLI | rs10488764 |
| Exac | rs10488764 |
| Gnomad | rs10488764 |
| Varsome | rs10488764 |
| LitVar | rs10488764 |
| Map | rs10488764 |
| PheGenI | rs10488764 |
| Biobank | rs10488764 |
| 1000 genomes | rs10488764 |
| hgdp | rs10488764 |
| ensembl | rs10488764 |
| geneview | rs10488764 |
| scholar | rs10488764 |
| rs10488764 | |
| pharmgkb | rs10488764 |
| gwascentral | rs10488764 |
| openSNP | rs10488764 |
| 23andMe | rs10488764 |
| SNPshot | rs10488764 |
| SNPdbe | rs10488764 |
| MSV3d | rs10488764 |
| GWAS Ctlg | rs10488764 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26370181] Association between CCDC132, FDX1 and TNFSF13 gene polymorphisms and the risk of IgA nephropathy
[PMID 26431901] Genetic polymorphisms in TNFSF13 and FDX1 are associated with IgA nephropathy in the Han Chinese population
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- 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
