rs1679013
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1679013(C;C) |
Make rs1679013(C;T) |
Make rs1679013(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 22206988 |
is a | snp |
is | mentioned by |
dbSNP | rs1679013 |
dbSNP (classic) | rs1679013 |
ClinGen | rs1679013 |
ebi | rs1679013 |
HLI | rs1679013 |
Exac | rs1679013 |
Gnomad | rs1679013 |
Varsome | rs1679013 |
LitVar | rs1679013 |
Map | rs1679013 |
PheGenI | rs1679013 |
Biobank | rs1679013 |
1000 genomes | rs1679013 |
hgdp | rs1679013 |
ensembl | rs1679013 |
geneview | rs1679013 |
scholar | rs1679013 |
rs1679013 | |
pharmgkb | rs1679013 |
gwascentral | rs1679013 |
openSNP | rs1679013 |
23andMe | rs1679013 |
SNPshot | rs1679013 |
SNPdbe | rs1679013 |
MSV3d | rs1679013 |
GWAS Ctlg | rs1679013 |
GMAF | 0.4871 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23770605![]() |
Trait | Chronic lymphocytic leukemia |
Title | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. |
Risk Allele | C |
P-val | 1E-8 |
Odds Ratio | 1.19 [1.12-1.27] |