rs9864370
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9864370(C;C) |
Make rs9864370(C;T) |
Make rs9864370(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 169198452 |
Gene | MECOM |
is a | snp |
is | mentioned by |
dbSNP | rs9864370 |
dbSNP (classic) | rs9864370 |
ClinGen | rs9864370 |
ebi | rs9864370 |
HLI | rs9864370 |
Exac | rs9864370 |
Gnomad | rs9864370 |
Varsome | rs9864370 |
LitVar | rs9864370 |
Map | rs9864370 |
PheGenI | rs9864370 |
Biobank | rs9864370 |
1000 genomes | rs9864370 |
hgdp | rs9864370 |
ensembl | rs9864370 |
geneview | rs9864370 |
scholar | rs9864370 |
rs9864370 | |
pharmgkb | rs9864370 |
gwascentral | rs9864370 |
openSNP | rs9864370 |
23andMe | rs9864370 |
SNPshot | rs9864370 |
SNPdbe | rs9864370 |
MSV3d | rs9864370 |
GWAS Ctlg | rs9864370 |
GMAF | 0.07438 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23502783] |
Trait | Multiple myeloma (hyperdiploidy) |
Title | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
Risk Allele | G |
P-val | 9E-6 |
Odds Ratio | 2.04 [1.49-2.80] |