rs13028485
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13028485(A;A) |
Make rs13028485(A;G) |
Make rs13028485(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 173640196 |
Gene | LOC107985961 |
is a | snp |
is | mentioned by |
dbSNP | rs13028485 |
dbSNP (classic) | rs13028485 |
ClinGen | rs13028485 |
ebi | rs13028485 |
HLI | rs13028485 |
Exac | rs13028485 |
Gnomad | rs13028485 |
Varsome | rs13028485 |
LitVar | rs13028485 |
Map | rs13028485 |
PheGenI | rs13028485 |
Biobank | rs13028485 |
1000 genomes | rs13028485 |
hgdp | rs13028485 |
ensembl | rs13028485 |
geneview | rs13028485 |
scholar | rs13028485 |
rs13028485 | |
pharmgkb | rs13028485 |
gwascentral | rs13028485 |
openSNP | rs13028485 |
23andMe | rs13028485 |
SNPshot | rs13028485 |
SNPdbe | rs13028485 |
MSV3d | rs13028485 |
GWAS Ctlg | rs13028485 |
GMAF | 0.1116 |
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 | 2.17 [1.57-2.99] |