rs1449572
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1449572(A;A) |
Make rs1449572(A;C) |
Make rs1449572(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 48892795 |
Gene | LOC107984559 |
is a | snp |
is | mentioned by |
dbSNP | rs1449572 |
dbSNP (classic) | rs1449572 |
ClinGen | rs1449572 |
ebi | rs1449572 |
HLI | rs1449572 |
Exac | rs1449572 |
Gnomad | rs1449572 |
Varsome | rs1449572 |
LitVar | rs1449572 |
Map | rs1449572 |
PheGenI | rs1449572 |
Biobank | rs1449572 |
1000 genomes | rs1449572 |
hgdp | rs1449572 |
ensembl | rs1449572 |
geneview | rs1449572 |
scholar | rs1449572 |
rs1449572 | |
pharmgkb | rs1449572 |
gwascentral | rs1449572 |
openSNP | rs1449572 |
23andMe | rs1449572 |
SNPshot | rs1449572 |
SNPdbe | rs1449572 |
MSV3d | rs1449572 |
GWAS Ctlg | rs1449572 |
GMAF | 0.1882 |
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 | 8E-6 |
Odds Ratio | 1.73 [1.36-2.21] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d