rs4521323
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4521323(A;A) |
Make rs4521323(A;C) |
Make rs4521323(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 173734763 |
Gene | LOC101928478 |
is a | snp |
is | mentioned by |
dbSNP | rs4521323 |
dbSNP (classic) | rs4521323 |
ClinGen | rs4521323 |
ebi | rs4521323 |
HLI | rs4521323 |
Exac | rs4521323 |
Gnomad | rs4521323 |
Varsome | rs4521323 |
LitVar | rs4521323 |
Map | rs4521323 |
PheGenI | rs4521323 |
Biobank | rs4521323 |
1000 genomes | rs4521323 |
hgdp | rs4521323 |
ensembl | rs4521323 |
geneview | rs4521323 |
scholar | rs4521323 |
rs4521323 | |
pharmgkb | rs4521323 |
gwascentral | rs4521323 |
openSNP | rs4521323 |
23andMe | rs4521323 |
SNPshot | rs4521323 |
SNPdbe | rs4521323 |
MSV3d | rs4521323 |
GWAS Ctlg | rs4521323 |
GMAF | 0.4275 |
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 | C |
P-val | 9E-6 |
Odds Ratio | 1.28 [1.15-1.43] |