rs12638862
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12638862(A;A) |
Make rs12638862(A;G) |
Make rs12638862(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 169759718 |
is a | snp |
is | mentioned by |
dbSNP | rs12638862 |
dbSNP (classic) | rs12638862 |
ClinGen | rs12638862 |
ebi | rs12638862 |
HLI | rs12638862 |
Exac | rs12638862 |
Gnomad | rs12638862 |
Varsome | rs12638862 |
LitVar | rs12638862 |
Map | rs12638862 |
PheGenI | rs12638862 |
Biobank | rs12638862 |
1000 genomes | rs12638862 |
hgdp | rs12638862 |
ensembl | rs12638862 |
geneview | rs12638862 |
scholar | rs12638862 |
rs12638862 | |
pharmgkb | rs12638862 |
gwascentral | rs12638862 |
openSNP | rs12638862 |
23andMe | rs12638862 |
SNPshot | rs12638862 |
SNPdbe | rs12638862 |
MSV3d | rs12638862 |
GWAS Ctlg | rs12638862 |
GMAF | 0.3306 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23502783![]() |
Trait | Multiple myeloma (IgH translocation) |
Title | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
Risk Allele | A |
P-val | 2E-6 |
Odds Ratio | 1.37 [1.20-1.56] |