rs6746082
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6746082(A;A) |
| Make rs6746082(A;C) |
| Make rs6746082(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 25436375 |
| Gene | DTNB, LOC101929272 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6746082 |
| dbSNP (classic) | rs6746082 |
| ClinGen | rs6746082 |
| ebi | rs6746082 |
| HLI | rs6746082 |
| Exac | rs6746082 |
| Gnomad | rs6746082 |
| Varsome | rs6746082 |
| LitVar | rs6746082 |
| Map | rs6746082 |
| PheGenI | rs6746082 |
| Biobank | rs6746082 |
| 1000 genomes | rs6746082 |
| hgdp | rs6746082 |
| ensembl | rs6746082 |
| geneview | rs6746082 |
| scholar | rs6746082 |
| rs6746082 | |
| pharmgkb | rs6746082 |
| gwascentral | rs6746082 |
| openSNP | rs6746082 |
| 23andMe | rs6746082 |
| SNPshot | rs6746082 |
| SNPdbe | rs6746082 |
| MSV3d | rs6746082 |
| GWAS Ctlg | rs6746082 |
| GMAF | 0.405 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22120009 |
| Trait | |
| Title | Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. |
| Risk Allele | A |
| P-val | 4E-7 |
| Odds Ratio | 1.2900 None |
[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- 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
