rs730566
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs730566(G;G) |
| Make rs730566(G;T) |
| Make rs730566(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 48445644 |
| Gene | ATRIP, CCDC51 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs730566 |
| dbSNP (classic) | rs730566 |
| ClinGen | rs730566 |
| ebi | rs730566 |
| HLI | rs730566 |
| Exac | rs730566 |
| Gnomad | rs730566 |
| Varsome | rs730566 |
| LitVar | rs730566 |
| Map | rs730566 |
| PheGenI | rs730566 |
| Biobank | rs730566 |
| 1000 genomes | rs730566 |
| hgdp | rs730566 |
| ensembl | rs730566 |
| geneview | rs730566 |
| scholar | rs730566 |
| rs730566 | |
| pharmgkb | rs730566 |
| gwascentral | rs730566 |
| openSNP | rs730566 |
| 23andMe | rs730566 |
| SNPshot | rs730566 |
| SNPdbe | rs730566 |
| MSV3d | rs730566 |
| GWAS Ctlg | rs730566 |
| GMAF | 0.3384 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22210626 |
| Trait | |
| Title | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | 1.2700 None |
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
