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rs2647046

From SNPedia

Orientationplus
Stabilizedplus
Make rs2647046(A;A)
Make rs2647046(A;C)
Make rs2647046(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position32700559
is asnp
is mentioned by
dbSNPrs2647046
ebirs2647046
HLIrs2647046
Exacrs2647046
Varsomers2647046
Maprs2647046
PheGenIrs2647046
hapmaprs2647046
1000 genomesrs2647046
hgdprs2647046
ensemblrs2647046
gopubmedrs2647046
geneviewrs2647046
scholarrs2647046
googlers2647046
pharmgkbrs2647046
gwascentralrs2647046
openSNPrs2647046
23andMers2647046
23andMe allrs2647046
SNP Nexus

SNPshotrs2647046
SNPdbers2647046
MSV3drs2647046
GWAS Ctlgrs2647046
GMAF0.2948
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23349640OA-icon.png]
Trait Lymphoma
Title Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.
Risk Allele
P-val 2E-6
Odds Ratio 1.25 [1.14-1.37]


[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


[PMID 20546594OA-icon.png] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.


[PMID 25308886] Functional relevance for multiple sclerosis-associated genetic variants