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rs6773854

From SNPedia

Orientationplus
Stabilizedplus
Make rs6773854(C;C)
Make rs6773854(C;T)
Make rs6773854(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position187931631
is asnp
is mentioned by
dbSNPrs6773854
ebirs6773854
HLIrs6773854
Exacrs6773854
Varsomers6773854
Maprs6773854
PheGenIrs6773854
hapmaprs6773854
1000 genomesrs6773854
hgdprs6773854
ensemblrs6773854
gopubmedrs6773854
geneviewrs6773854
scholarrs6773854
googlers6773854
pharmgkbrs6773854
gwascentralrs6773854
openSNPrs6773854
23andMers6773854
23andMe allrs6773854
SNP Nexus

SNPshotrs6773854
SNPdbers6773854
MSV3drs6773854
GWAS Ctlgrs6773854
GMAF0.2121
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23749188]
Trait B cell non-Hodgkin lymphoma
Title Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population.
Risk Allele C
P-val 3E-13
Odds Ratio 1.44 [1.31-1.59]