rs4629710
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4629710(A;A) |
Make rs4629710(A;G) |
Make rs4629710(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 131242437 |
Gene | AKAP7 |
is a | snp |
is | mentioned by |
dbSNP | rs4629710 |
dbSNP (classic) | rs4629710 |
ClinGen | rs4629710 |
ebi | rs4629710 |
HLI | rs4629710 |
Exac | rs4629710 |
Gnomad | rs4629710 |
Varsome | rs4629710 |
LitVar | rs4629710 |
Map | rs4629710 |
PheGenI | rs4629710 |
Biobank | rs4629710 |
1000 genomes | rs4629710 |
hgdp | rs4629710 |
ensembl | rs4629710 |
geneview | rs4629710 |
scholar | rs4629710 |
rs4629710 | |
pharmgkb | rs4629710 |
gwascentral | rs4629710 |
openSNP | rs4629710 |
23andMe | rs4629710 |
SNPshot | rs4629710 |
SNPdbe | rs4629710 |
MSV3d | rs4629710 |
GWAS Ctlg | rs4629710 |
GMAF | 0.09917 |
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 | 6E-6 |
Odds Ratio | 1.60 [1.31-1.96] |