rs4737547
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4737547(A;A) |
Make rs4737547(A;G) |
Make rs4737547(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 59633105 |
is a | snp |
is | mentioned by |
dbSNP | rs4737547 |
dbSNP (classic) | rs4737547 |
ClinGen | rs4737547 |
ebi | rs4737547 |
HLI | rs4737547 |
Exac | rs4737547 |
Gnomad | rs4737547 |
Varsome | rs4737547 |
LitVar | rs4737547 |
Map | rs4737547 |
PheGenI | rs4737547 |
Biobank | rs4737547 |
1000 genomes | rs4737547 |
hgdp | rs4737547 |
ensembl | rs4737547 |
geneview | rs4737547 |
scholar | rs4737547 |
rs4737547 | |
pharmgkb | rs4737547 |
gwascentral | rs4737547 |
openSNP | rs4737547 |
23andMe | rs4737547 |
SNPshot | rs4737547 |
SNPdbe | rs4737547 |
MSV3d | rs4737547 |
GWAS Ctlg | rs4737547 |
GMAF | 0.4541 |
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 | G |
P-val | 3E-6 |
Odds Ratio | 1.30 [1.17-1.45] |