rs2086824
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2086824(A;A) |
Make rs2086824(A;C) |
Make rs2086824(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 89404838 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs2086824 |
dbSNP (classic) | rs2086824 |
ClinGen | rs2086824 |
ebi | rs2086824 |
HLI | rs2086824 |
Exac | rs2086824 |
Gnomad | rs2086824 |
Varsome | rs2086824 |
LitVar | rs2086824 |
Map | rs2086824 |
PheGenI | rs2086824 |
Biobank | rs2086824 |
1000 genomes | rs2086824 |
hgdp | rs2086824 |
ensembl | rs2086824 |
geneview | rs2086824 |
scholar | rs2086824 |
rs2086824 | |
pharmgkb | rs2086824 |
gwascentral | rs2086824 |
openSNP | rs2086824 |
23andMe | rs2086824 |
SNPshot | rs2086824 |
SNPdbe | rs2086824 |
MSV3d | rs2086824 |
GWAS Ctlg | rs2086824 |
GMAF | 0.2498 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 1.58 [1.31-1.91] |