Have questions? Visit https://www.reddit.com/r/SNPedia

rs2456449

From SNPedia

Orientationplus
Stabilizedplus
Make rs2456449(A;A)
Make rs2456449(A;G)
Make rs2456449(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127180736
is asnp
is mentioned by
dbSNPrs2456449
ebirs2456449
HLIrs2456449
Exacrs2456449
Varsomers2456449
Maprs2456449
PheGenIrs2456449
hapmaprs2456449
1000 genomesrs2456449
hgdprs2456449
ensemblrs2456449
gopubmedrs2456449
geneviewrs2456449
scholarrs2456449
googlers2456449
pharmgkbrs2456449
gwascentralrs2456449
openSNPrs2456449
23andMers2456449
23andMe allrs2456449
SNP Nexus

SNPshotrs2456449
SNPdbers2456449
MSV3drs2456449
GWAS Ctlgrs2456449
GMAF0.3228
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062064]
Trait Chronic lymphocytic leukemia
Title Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk
Risk Allele G
P-val 8E-10
Odds Ratio 1.26 [1.17-1.35]


[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis