rs2019960
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2019960(C;C) |
Make rs2019960(C;T) |
Make rs2019960(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 128180025 |
is a | snp |
is | mentioned by |
dbSNP | rs2019960 |
dbSNP (classic) | rs2019960 |
ClinGen | rs2019960 |
ebi | rs2019960 |
HLI | rs2019960 |
Exac | rs2019960 |
Gnomad | rs2019960 |
Varsome | rs2019960 |
LitVar | rs2019960 |
Map | rs2019960 |
PheGenI | rs2019960 |
Biobank | rs2019960 |
1000 genomes | rs2019960 |
hgdp | rs2019960 |
ensembl | rs2019960 |
geneview | rs2019960 |
scholar | rs2019960 |
rs2019960 | |
pharmgkb | rs2019960 |
gwascentral | rs2019960 |
openSNP | rs2019960 |
23andMe | rs2019960 |
SNPshot | rs2019960 |
SNPdbe | rs2019960 |
MSV3d | rs2019960 |
GWAS Ctlg | rs2019960 |
GMAF | 0.2433 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21037568] A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)
GWAS snp | |
---|---|
PMID | [PMID 21833088] |
Trait | |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | G |
P-val | 5E-9 |
Odds Ratio | 1.1200 [1.10-1.13] |
GWAS snp | |
---|---|
PMID | [PMID 24149102] |
Trait | Hodgkin's lymphoma |
Title | Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. |
Risk Allele | G |
P-val | 6E-10 |
Odds Ratio | 1.37 [NR] |
GWAS snp | |
---|---|
PMID | [PMID 24920014] |
Trait | Hodgkin's lymphoma |
Title | A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. |
Risk Allele | C |
P-val | 7E-8 |
Odds Ratio | 1.30 [1.181.43] |