rs7086888
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7086888(A;A) |
Make rs7086888(A;G) |
Make rs7086888(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 4634004 |
is a | snp |
is | mentioned by |
dbSNP | rs7086888 |
dbSNP (classic) | rs7086888 |
ClinGen | rs7086888 |
ebi | rs7086888 |
HLI | rs7086888 |
Exac | rs7086888 |
Gnomad | rs7086888 |
Varsome | rs7086888 |
LitVar | rs7086888 |
Map | rs7086888 |
PheGenI | rs7086888 |
Biobank | rs7086888 |
1000 genomes | rs7086888 |
hgdp | rs7086888 |
ensembl | rs7086888 |
geneview | rs7086888 |
scholar | rs7086888 |
rs7086888 | |
pharmgkb | rs7086888 |
gwascentral | rs7086888 |
openSNP | rs7086888 |
23andMe | rs7086888 |
SNPshot | rs7086888 |
SNPdbe | rs7086888 |
MSV3d | rs7086888 |
GWAS Ctlg | rs7086888 |
GMAF | 0.1047 |
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 | 8E-6 |
Odds Ratio | 1.87 [1.42-2.46] |