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rs6683977

From SNPedia

Orientationplus
Stabilizedplus
Make rs6683977(C;C)
Make rs6683977(C;G)
Make rs6683977(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position66303417
GenePDE4B
is asnp
is mentioned by
dbSNPrs6683977
ebirs6683977
HLIrs6683977
Exacrs6683977
Varsomers6683977
Maprs6683977
PheGenIrs6683977
hapmaprs6683977
1000 genomesrs6683977
hgdprs6683977
ensemblrs6683977
gopubmedrs6683977
geneviewrs6683977
scholarrs6683977
googlers6683977
pharmgkbrs6683977
gwascentralrs6683977
openSNPrs6683977
23andMers6683977
23andMe allrs6683977
SNP Nexus

SNPshotrs6683977
SNPdbers6683977
MSV3drs6683977
GWAS Ctlgrs6683977
GMAF0.3108
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23007406OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele C
P-val 5E-6
Odds Ratio 1.41 [1.22-1.64]