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rs4987852

From SNPedia

Orientationminus
Stabilizedplus
Make rs4987852(A;A)
Make rs4987852(A;G)
Make rs4987852(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position63126688
GeneBCL2
is asnp
is mentioned by
dbSNPrs4987852
ebirs4987852
HLIrs4987852
Exacrs4987852
Varsomers4987852
Maprs4987852
PheGenIrs4987852
hapmaprs4987852
1000 genomesrs4987852
hgdprs4987852
ensemblrs4987852
gopubmedrs4987852
geneviewrs4987852
scholarrs4987852
googlers4987852
pharmgkbrs4987852
gwascentralrs4987852
openSNPrs4987852
23andMers4987852
23andMe allrs4987852
SNP Nexus

SNPshotrs4987852
SNPdbers4987852
MSV3drs4987852
GWAS Ctlgrs4987852
GMAF0.02801
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele
P-val 8E-11
Odds Ratio 1.41 [NR]


[PMID 22037783] Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer.