rs10180663
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10180663(C;C) |
Make rs10180663(C;T) |
Make rs10180663(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 25410373 |
Gene | DTNB |
is a | snp |
is | mentioned by |
dbSNP | rs10180663 |
dbSNP (classic) | rs10180663 |
ClinGen | rs10180663 |
ebi | rs10180663 |
HLI | rs10180663 |
Exac | rs10180663 |
Gnomad | rs10180663 |
Varsome | rs10180663 |
LitVar | rs10180663 |
Map | rs10180663 |
PheGenI | rs10180663 |
Biobank | rs10180663 |
1000 genomes | rs10180663 |
hgdp | rs10180663 |
ensembl | rs10180663 |
geneview | rs10180663 |
scholar | rs10180663 |
rs10180663 | |
pharmgkb | rs10180663 |
gwascentral | rs10180663 |
openSNP | rs10180663 |
23andMe | rs10180663 |
SNPshot | rs10180663 |
SNPdbe | rs10180663 |
MSV3d | rs10180663 |
GWAS Ctlg | rs10180663 |
GMAF | 0.472 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 1.64 [1.34-2.02] |