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